Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionsodium ion binding

SCN1A SCN2A SCN3A SCN8A

1.10e-0814384GO:0031402
GeneOntologyMolecularFunctionvoltage-gated sodium channel activity

SCN1A SCN2A SCN3A SCN8A

1.62e-0726384GO:0005248
GeneOntologyMolecularFunctionalkali metal ion binding

SCN1A SCN2A SCN3A SCN8A

1.62e-0726384GO:0031420
GeneOntologyMolecularFunctionsodium channel activity

SCN1A SCN2A SCN3A SCN8A

2.83e-0652384GO:0005272
GeneOntologyMolecularFunctionsodium ion transmembrane transporter activity

SCN1A SCN2A SCN3A SCN8A

3.05e-04171384GO:0015081
GeneOntologyMolecularFunctionvoltage-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential

SCN1A SCN2A

4.71e-0417382GO:0099508
GeneOntologyMolecularFunctionhistone H3K4 methyltransferase activity

KMT2B ASH1L

6.56e-0420382GO:0042800
GeneOntologyMolecularFunctionprotein domain specific binding

BLNK POU3F3 SP100 TACC1 PRKDC CARD8 SCN2A

1.16e-03875387GO:0019904
GeneOntologyBiologicalProcessmembrane depolarization during action potential

SCN1A SCN2A SCN3A SCN8A

4.95e-0736374GO:0086010
GeneOntologyBiologicalProcessmembrane depolarization

GCLC SCN1A SCN2A SCN3A SCN8A

2.40e-06121375GO:0051899
GeneOntologyBiologicalProcesscardiac muscle cell action potential involved in contraction

SCN1A SCN2A SCN3A SCN8A

4.54e-0662374GO:0086002
GeneOntologyBiologicalProcessneuronal action potential

SCN1A SCN2A SCN3A SCN8A

4.84e-0663374GO:0019228
GeneOntologyBiologicalProcesscardiac muscle cell action potential

SCN1A SCN2A SCN3A SCN8A

1.75e-0587374GO:0086001
GeneOntologyBiologicalProcesscardiac muscle cell contraction

SCN1A SCN2A SCN3A SCN8A

2.28e-0593374GO:0086003
GeneOntologyBiologicalProcessaction potential

FOXP1 SCN1A SCN2A SCN3A SCN8A

2.83e-05201375GO:0001508
GeneOntologyBiologicalProcessnerve development

MNX1 SCN1A SCN2A SCN8A

4.26e-05109374GO:0021675
GeneOntologyBiologicalProcesstransmission of nerve impulse

SCN1A SCN2A SCN3A SCN8A

4.74e-05112374GO:0019226
GeneOntologyBiologicalProcessactin-mediated cell contraction

SCN1A SCN2A SCN3A SCN8A

7.73e-05127374GO:0070252
GeneOntologyBiologicalProcessbrain development

PITPNM1 FOXP1 POU3F3 DMXL2 TACC1 PRKDC PTF1A SCN2A

1.15e-04859378GO:0007420
GeneOntologyBiologicalProcessimmunoglobulin V(D)J recombination

FOXP1 PRKDC

1.40e-0410372GO:0033152
GeneOntologyBiologicalProcessactin filament-based movement

SCN1A SCN2A SCN3A SCN8A

1.59e-04153374GO:0030048
GeneOntologyBiologicalProcesshead development

PITPNM1 FOXP1 POU3F3 DMXL2 TACC1 PRKDC PTF1A SCN2A

1.84e-04919378GO:0060322
GeneOntologyBiologicalProcesscentral nervous system development

PITPNM1 FOXP1 POU3F3 DMXL2 TACC1 PRKDC MNX1 PTF1A SCN2A

2.06e-041197379GO:0007417
GeneOntologyBiologicalProcesscardiac muscle contraction

SCN1A SCN2A SCN3A SCN8A

2.22e-04167374GO:0060048
GeneOntologyBiologicalProcesstelencephalon development

FOXP1 POU3F3 DMXL2 TACC1 SCN2A

2.99e-04332375GO:0021537
GeneOntologyBiologicalProcesscellular response to antibiotic

PLA2G4A SCN3A

3.70e-0416372GO:0071236
GeneOntologyBiologicalProcessregulation of membrane potential

FOXP1 GCLC SCN1A SCN2A SCN3A SCN8A

4.39e-04559376GO:0042391
GeneOntologyBiologicalProcesssodium ion transmembrane transport

SCN1A SCN2A SCN3A SCN8A

5.11e-04208374GO:0035725
GeneOntologyBiologicalProcessstriated muscle contraction

SCN1A SCN2A SCN3A SCN8A

5.99e-04217374GO:0006941
GeneOntologyBiologicalProcesspositive regulation of immune response

BLNK PLA2G4A FOXP1 PRKDC GBP4 FCHO1 CARD8

6.63e-04845377GO:0050778
GeneOntologyBiologicalProcessV(D)J recombination

FOXP1 PRKDC

7.74e-0423372GO:0033151
GeneOntologyBiologicalProcessnegative regulation of cilium assembly

KIF24 WDR44

7.74e-0423372GO:1902018
GeneOntologyBiologicalProcessactivation of immune response

BLNK FOXP1 PRKDC GBP4 FCHO1 CARD8

7.76e-04623376GO:0002253
GeneOntologyBiologicalProcessovulation

PLA2G4A KMT2B

8.43e-0424372GO:0030728
GeneOntologyBiologicalProcessimmature B cell differentiation

FOXP1 PRKDC

9.15e-0425372GO:0002327
GeneOntologyBiologicalProcessblood circulation

ARHGEF12 GCLC SCN1A SCN2A SCN3A SCN8A

9.52e-04648376GO:0008015
GeneOntologyCellularComponentvoltage-gated sodium channel complex

SCN1A SCN2A SCN3A SCN8A

2.17e-0817384GO:0001518
GeneOntologyCellularComponentsodium channel complex

SCN1A SCN2A SCN3A SCN8A

2.13e-0729384GO:0034706
GeneOntologyCellularComponentnode of Ranvier

SCN1A SCN2A SCN8A

6.18e-0620383GO:0033268
GeneOntologyCellularComponentaxon initial segment

SCN1A SCN2A SCN8A

1.96e-0529383GO:0043194
GeneOntologyCellularComponentmain axon

SCN1A SCN2A SCN8A

5.65e-0489383GO:0044304
GeneOntologyCellularComponentcation channel complex

SCN1A SCN2A SCN3A SCN8A

8.51e-04235384GO:0034703
HumanPhenoSimple febrile seizure

SCN1A SCN2A SCN3A SCN8A

1.82e-0627184HP:0011171
HumanPhenoGeneralized clonic seizure

DMXL2 SCN1A SCN2A SCN8A

4.74e-0634184HP:0011169
HumanPhenoClonic seizure

DMXL2 SCN1A SCN2A SCN3A SCN8A

6.54e-0681185HP:0020221
HumanPhenoFocal automatism seizure

SCN1A SCN2A SCN8A

7.99e-0612183HP:0032898
HumanPhenoFocal clonic seizure

DMXL2 SCN1A SCN2A SCN8A

1.12e-0542184HP:0002266
HumanPhenoComplex febrile seizure

SCN1A SCN2A SCN8A

2.02e-0516183HP:0011172
HumanPhenoChoreoathetosis

POU3F3 DMXL2 SCN1A SCN2A SCN8A

5.04e-05123185HP:0001266
HumanPhenoGeneralized tonic seizure

DMXL2 SCN1A SCN2A SCN8A

6.08e-0564184HP:0010818
HumanPhenoMultifocal epileptiform discharges

DMXL2 SCN1A SCN2A SCN8A

6.86e-0566184HP:0010841
HumanPhenoFocal hemiclonic seizure

SCN1A SCN2A SCN8A

8.12e-0525183HP:0006813
HumanPhenoAbnormal myelination

FOXP1 POU3F3 DMXL2 PRKDC SCN1A SCN2A SCN3A SCN8A ASH1L

9.96e-05622189HP:0012447
HumanPhenoInfection-related seizure

DMXL2 SCN1A SCN2A SCN3A SCN8A

1.11e-04145185HP:0032892
HumanPhenoSeizure precipitated by febrile infection

DMXL2 SCN1A SCN2A SCN3A SCN8A

1.11e-04145185HP:0032894
HumanPhenoFebrile seizure (within the age range of 3 months to 6 years)

DMXL2 SCN1A SCN2A SCN3A SCN8A

1.11e-04145185HP:0002373
HumanPhenoFocal head nodding automatism seizure

SCN2A SCN8A

1.17e-045182HP:0032906
HumanPhenoNeonatal electro-clinical non-motor seizure

SCN2A SCN8A

1.17e-045182HP:0032812
HumanPhenoNeonatal seizure with electrographic correlate

SCN2A SCN8A

1.17e-045182HP:0032808
HumanPhenoNeonatal electro-clinical seizure

SCN2A SCN8A

1.17e-045182HP:0032809
HumanPhenoNeonatal electro-clinical seizure with behavior arrest

SCN2A SCN8A

1.17e-045182HP:0032823
HumanPhenoCompulsive behaviors

FOXP1 SCN1A SCN2A SCN8A ASH1L

1.66e-04158185HP:0000722
HumanPhenoNormal interictal EEG

SCN2A SCN8A

1.75e-046182HP:0002372
HumanPhenoObsessive-compulsive trait

SCN1A SCN2A ASH1L

1.89e-0433183HP:0008770
HumanPhenoAutistic behavior

FOXP1 POU3F3 DMXL2 KMT2B SCN1A SCN2A SCN3A SCN8A ASH1L

1.97e-04678189HP:0000729
HumanPhenoAthetosis

POU3F3 DMXL2 SCN1A SCN2A SCN8A

2.10e-04166185HP:0002305
HumanPhenoEEG with spike-wave complexes

DMXL2 SCN1A SCN2A SCN8A

2.12e-0488184HP:0010850
HumanPhenoEyelid myoclonia seizure

SCN2A SCN8A

2.45e-047182HP:0032678
HumanPhenoDelayed myelination

FOXP1 POU3F3 DMXL2 SCN1A SCN2A ASH1L

2.77e-04280186HP:0012448
HumanPhenoHyperactivity

FOXP1 DMXL2 KMT2B SCN1A SCN2A SCN3A SCN8A ASH1L

3.18e-04558188HP:0000752
HumanPhenoPhotosensitive myoclonic seizure

SCN1A SCN2A

3.26e-048182HP:0001327
HumanPhenoCyanotic episode

SCN1A SCN2A

3.26e-048182HP:0200048
HumanPhenoFocal non-motor seizure

SCN1A SCN2A SCN8A

3.37e-0440183HP:0032679
HumanPhenoHypsarrhythmia

DMXL2 SCN1A SCN2A SCN3A SCN8A

3.49e-04185185HP:0002521
HumanPhenoDiagnostic behavioral phenotype

FOXP1 POU3F3 DMXL2 KMT2B SCN1A SCN2A SCN3A SCN8A ASH1L

4.18e-04747189HP:0025783
HumanPhenoSudden unexpected death in epilepsy

SCN1A SCN8A

5.22e-0410182HP:0033258
HumanPhenoLimited neck range of motion

SCN1A SCN2A

6.37e-0411182HP:0000466
HumanPhenoNeonatal seizure

SCN2A SCN8A

6.37e-0411182HP:0032807
HumanPhenoEEG with focal epileptiform discharges

DMXL2 SCN1A SCN2A SCN8A

6.51e-04118184HP:0011185
HumanPhenoEpileptic encephalopathy

SCN1A SCN2A SCN3A SCN8A

6.72e-04119184HP:0200134
HumanPhenoBilateral tonic-clonic seizure with focal onset

SCN1A SCN2A SCN8A

7.35e-0452183HP:0007334
HumanPhenoEpilepsia partialis continua

SCN1A SCN2A

7.62e-0412182HP:0012847
HumanPhenoFocal impaired awareness seizure

SCN1A SCN2A SCN3A SCN8A

8.34e-04126184HP:0002384
HumanPhenoGeneralized cerebral atrophy/hypoplasia

SCN1A SCN2A

8.99e-0413182HP:0007058
HumanPhenoFocal motor seizure

DMXL2 SCN1A SCN2A SCN8A

9.66e-04131184HP:0011153
HumanPhenoAortopulmonary collateral arteries

SCN1A SCN2A

1.21e-0315182HP:0031834
HumanPhenoPhotosensitive tonic-clonic seizure

SCN1A SCN2A

1.21e-0315182HP:0007207
HumanPhenoFacial tics

SCN1A SCN2A

1.21e-0315182HP:0011468
HumanPhenoTonic seizure

DMXL2 SCN1A SCN2A SCN8A

1.24e-03140184HP:0032792
HumanPhenoMyoclonus

DMXL2 KMT2B SCN1A SCN2A SCN3A SCN8A

1.25e-03371186HP:0001336
HumanPhenoChorea

POU3F3 DMXL2 SCN1A SCN2A SCN8A

1.33e-03248185HP:0002072
HumanPhenoDysgenesis of the hippocampus

SCN1A SCN2A

1.37e-0316182HP:0025101
HumanPhenoDialeptic seizure

DMXL2 SCN1A SCN2A SCN3A SCN8A

1.41e-03251185HP:0011146
HumanPhenoAtypical absence status epilepticus

SCN1A SCN2A

1.55e-0317182HP:0011151
HumanPhenoFocal motor status epilepticus

SCN1A SCN2A

1.55e-0317182HP:0032663
HumanPhenoFocal emotional seizure with laughing

SCN1A SCN2A

1.55e-0317182HP:0010821
HumanPhenoImpulsivity

SCN1A SCN2A SCN3A SCN8A

1.56e-03149184HP:0100710
HumanPhenoUni- and bilateral multifocal epileptiform discharges

DMXL2 SCN2A

1.75e-0318182HP:0011190
HumanPhenoVisually-induced seizure

SCN1A SCN2A

1.75e-0318182HP:0020216
HumanPhenoGeneralized non-convulsive status epilepticus without coma

SCN1A SCN2A

1.75e-0318182HP:0032860
HumanPhenoFocal emotional seizure

SCN1A SCN2A

1.75e-0318182HP:0025613
HumanPhenoEEG with generalized epileptiform discharges

DMXL2 SCN1A SCN2A SCN3A SCN8A

1.95e-03270185HP:0011198
HumanPhenoDrooling

FOXP1 POU3F3 SCN1A SCN2A

2.08e-03161184HP:0002307
HumanPhenoProtein-losing enteropathy

BLNK CARD8

2.16e-0320182HP:0002243
HumanPhenoNon-convulsive status epilepticus without coma

SCN1A SCN2A

2.16e-0320182HP:0032671
HumanPhenoPsychomotor deterioration

SCN2A SCN8A

2.16e-0320182HP:0002361
HumanPhenoAbsent thumbnail

DMXL2 SCN2A

2.16e-0320182HP:0012554
HumanPhenoBrain imaging abnormality

FOXP1 SCN1A SCN2A SCN8A

2.38e-03167184HP:0410263
HumanPhenoTalipes valgus

SCN1A SCN2A

2.38e-0321182HP:0004684
HumanPhenoExcessive salivation

FOXP1 POU3F3 SCN1A SCN2A

2.54e-03170184HP:0003781
HumanPhenoFocal sensory seizure

SCN1A SCN8A

2.61e-0322182HP:0011157
HumanPhenoReflex seizure

SCN1A SCN2A

2.61e-0322182HP:0020207
HumanPhenoB-cell lymphoma

FOXP1 FCHO1

2.61e-0322182HP:0012191
HumanPhenoAbnormal small intestine morphology

BLNK PLA2G4A GCLC PTF1A CARD8

2.64e-03289185HP:0002244
DomainNa_trans_cytopl

SCN1A SCN2A SCN3A SCN8A

1.95e-106374PF11933
DomainNa_trans_cytopl

SCN1A SCN2A SCN3A SCN8A

1.95e-106374IPR024583
DomainNa_channel_asu

SCN1A SCN2A SCN3A SCN8A

2.71e-0910374IPR001696
DomainNa_trans_assoc

SCN1A SCN2A SCN3A SCN8A

2.71e-0910374IPR010526
DomainNa_trans_assoc

SCN1A SCN2A SCN3A SCN8A

2.71e-0910374PF06512
DomainChannel_four-helix_dom

SCN1A SCN2A SCN3A SCN8A

4.78e-0657374IPR027359
Domain-

SCN1A SCN2A SCN3A SCN8A

4.78e-06573741.20.120.350
DomainIQ

SCN1A SCN2A SCN3A SCN8A

1.94e-0581374SM00015
DomainIQ_motif_EF-hand-BS

SCN1A SCN2A SCN3A SCN8A

2.95e-0590374IPR000048
DomainIQ

SCN1A SCN2A SCN3A SCN8A

3.35e-0593374PS50096
DomainIon_trans_dom

SCN1A SCN2A SCN3A SCN8A

7.44e-05114374IPR005821
DomainIon_trans

SCN1A SCN2A SCN3A SCN8A

7.44e-05114374PF00520
DomainBAH

TNRC18 ASH1L

2.08e-0411372SM00439
DomainBAH

TNRC18 ASH1L

2.08e-0411372PF01426
DomainBAH_dom

TNRC18 ASH1L

2.08e-0411372IPR001025
DomainBAH

TNRC18 ASH1L

2.08e-0411372PS51038
DomainIQ

SCN1A SCN3A SCN8A

3.73e-0471373PF00612
DomainPost-SET_dom

KMT2B ASH1L

4.50e-0416372IPR003616
DomainPostSET

KMT2B ASH1L

4.50e-0416372SM00508
DomainPOST_SET

KMT2B ASH1L

4.50e-0416372PS50868
DomainAT_hook

KMT2B ASH1L

1.30e-0327372SM00384
DomainAT_hook_DNA-bd_motif

KMT2B ASH1L

1.30e-0327372IPR017956
DomainRGS

ARHGEF12 SNX25

2.70e-0339372IPR016137
DomainSET

KMT2B ASH1L

2.98e-0341372PF00856
DomainUBA

UBL7 SIK2

3.43e-0344372IPR015940
DomainSET

KMT2B ASH1L

3.74e-0346372SM00317
DomainUBA

UBL7 SIK2

3.90e-0347372PS50030
DomainSET_dom

KMT2B ASH1L

4.41e-0350372IPR001214
DomainSET

KMT2B ASH1L

4.41e-0350372PS50280
DomainPHD

KMT2B ASH1L

9.68e-0375372PF00628
DomainZnf_PHD-finger

KMT2B ASH1L

1.07e-0279372IPR019787
PathwayWP_DRAVET_SYNDROME

SCN1A SCN2A SCN3A SCN8A

3.78e-0728314M45519
PathwayREACTOME_INTERACTION_BETWEEN_L1_AND_ANKYRINS

SCN1A SCN2A SCN3A SCN8A

5.78e-0731314M877
PathwayREACTOME_PHASE_0_RAPID_DEPOLARISATION

SCN1A SCN2A SCN3A SCN8A

6.59e-0732314M27455
PathwayREACTOME_L1CAM_INTERACTIONS

SCN1A SCN2A SCN3A SCN8A

1.36e-04121314M872
PathwayWP_RETT_SYNDROME

SCN1A SCN2A SCN8A

1.56e-0448313M39759
PathwayREACTOME_CARDIAC_CONDUCTION

SCN1A SCN2A SCN3A SCN8A

1.79e-04130314M27454
PathwayWP_OMEGA3_OMEGA6_FATTY_ACID_SYNTHESIS

FADS2 PLA2G4A

4.83e-0415312M39789
PathwayWP_OMEGA3_OMEGA6_FATTY_ACID_SYNTHESIS

FADS2 PLA2G4A

5.51e-0416312MM15813
PathwayKEGG_ALPHA_LINOLENIC_ACID_METABOLISM

FADS2 PLA2G4A

7.82e-0419312M311
PathwayREACTOME_MUSCLE_CONTRACTION

SCN1A SCN2A SCN3A SCN8A

9.69e-04203314M5485
PathwayWP_ADHD_AND_AUTISM_ASD_PATHWAYS

ATG2A SCN1A SCN2A SCN3A SCN8A

1.13e-03367315M48346
Pubmed

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.

SCN1A SCN2A SCN3A SCN8A

1.21e-12438417537961
Pubmed

Sodium channel expression and transcript variation in the developing brain of human, Rhesus monkey, and mouse.

SCN1A SCN2A SCN3A SCN8A

1.21e-12438435031483
Pubmed

Abnormal changes in voltage-gated sodium channels subtypes NaV1.1, NaV1.2, NaV1.3, NaV1.6 and CaM/CaMKII pathway in low-grade astrocytoma.

SCN1A SCN2A SCN3A SCN8A

1.21e-12438429578003
Pubmed

A 'toothache tree' alkylamide inhibits Aδ mechanonociceptors to alleviate mechanical pain.

SCN1A SCN2A SCN3A SCN8A

1.81e-11638423652591
Pubmed

International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels.

SCN1A SCN2A SCN3A SCN8A

1.52e-10938416382098
Pubmed

Expression pattern of neuronal and skeletal muscle voltage-gated Na+ channels in the developing mouse heart.

SCN1A SCN2A SCN3A SCN8A

1.52e-10938415746173
Pubmed

Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice.

SCN1A SCN2A SCN3A SCN8A

5.96e-101238430175250
Pubmed

Regulation of neuronal voltage-gated sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2.

SCN1A SCN2A SCN3A SCN8A

8.60e-101338415123669
Pubmed

Sodium channels SCN1A, SCN2A and SCN3A in familial autism.

SCN1A SCN2A SCN3A

1.20e-09338312610651
Pubmed

SCN1A, SCN2A and SCN3A gene polymorphisms and responsiveness to antiepileptic drugs: a multicenter cohort study and meta-analysis.

SCN1A SCN2A SCN3A

1.20e-09338323859570
Pubmed

Multidrug resistance in epilepsy and polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, and SCN3A: correlation among phenotype, genotype, and mRNA expression.

SCN1A SCN2A SCN3A

1.20e-09338318784617
Pubmed

Characterization of 5' untranslated regions of the voltage-gated sodium channels SCN1A, SCN2A, and SCN3A and identification of cis-conserved noncoding sequences.

SCN1A SCN2A SCN3A

1.20e-09338317544618
Pubmed

Variable patterns of mutation density among NaV1.1, NaV1.2 and NaV1.6 point to channel-specific functional differences associated with childhood epilepsy.

SCN1A SCN2A SCN8A

1.20e-09338332845893
Pubmed

Comparison and optimization of in silico algorithms for predicting the pathogenicity of sodium channel variants in epilepsy.

SCN1A SCN2A SCN8A

1.20e-09338328518218
Pubmed

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy.

SCN1A SCN2A SCN8A

1.20e-09338317928448
Pubmed

Early expression of sodium channel transcripts and sodium current by cajal-retzius cells in the preplate of the embryonic mouse neocortex.

SCN1A SCN2A SCN3A

1.20e-09338314973256
Pubmed

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.

SCN1A SCN2A SCN8A

4.81e-09438321156207
Pubmed

Association of sodium voltage-gated channel genes polymorphisms with epilepsy risk and prognosis in the Saudi population.

SCN1A SCN2A SCN3A

4.81e-09438335801810
Pubmed

Use of recombinant inbred strains for studying genetic determinants of responses to alcohol.

SCN1A SCN2A SCN3A

4.81e-0943838974318
Pubmed

Three brain sodium channel alpha-subunit genes are clustered on the proximal segment of mouse chromosome 2.

SCN1A SCN2A SCN3A

1.20e-0853831679748
Pubmed

A new sodium channel alpha-subunit gene (Scn9a) from Schwann cells maps to the Scn1a, Scn2a, Scn3a cluster of mouse chromosome 2.

SCN1A SCN2A SCN3A

1.20e-0853838812438
Pubmed

Structure/function characterization of micro-conotoxin KIIIA, an analgesic, nearly irreversible blocker of mammalian neuronal sodium channels.

SCN2A SCN3A SCN8A

1.20e-08538317724025
Pubmed

Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy.

SCN1A SCN2A SCN3A

1.20e-08538324337656
Pubmed

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood.

SCN1A SCN2A SCN8A

4.20e-08738325818041
Pubmed

Quantitative trait loci mapping of genes that influence the sensitivity and tolerance to ethanol-induced hypothermia in BXD recombinant inbred mice.

SCN1A SCN2A SCN3A

2.63e-07123838169823
Pubmed

Confirmation of quantitative trait loci for alcohol preference in mice.

SCN1A SCN2A SCN3A

5.43e-07153839726281
Pubmed

Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures.

SCN1A SCN2A

1.16e-06238229649454
Pubmed

Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay.

SCN2A SCN3A

1.16e-06238220346423
Pubmed

Reduction of Kcnt1 is therapeutic in mouse models of SCN1A and SCN8A epilepsy.

SCN1A SCN8A

1.16e-06238237901435
Pubmed

An Scn1a epilepsy mutation in Scn8a alters seizure susceptibility and behavior.

SCN1A SCN8A

1.16e-06238226410685
Pubmed

Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice.

SCN1A SCN2A

1.16e-06238210827969
Pubmed

Differential role of sodium channels SCN1A and SCN2A gene polymorphisms with epilepsy and multiple drug resistance in the north Indian population.

SCN1A SCN2A

1.16e-06238219694741
Pubmed

Commonalities and distinctions between two neurodevelopmental disorder subtypes associated with SCN2A and SCN8A variants and literature review.

SCN2A SCN8A

1.16e-06238235348308
Pubmed

Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus.

SCN2A SCN3A

1.16e-06238211245985
Pubmed

Electrophysiological properties of two axonal sodium channels, Nav1.2 and Nav1.6, expressed in mouse spinal sensory neurones.

SCN2A SCN8A

1.16e-06238215760941
Pubmed

Differential expression of two sodium channel subtypes in human brain.

SCN1A SCN2A

1.16e-0623821317301
Pubmed

Duplication of the sodium channel gene cluster on 2q24 in children with early onset epilepsy.

SCN2A SCN3A

1.16e-06238223016767
Pubmed

Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual development.

SCN2A SCN3A

1.16e-06238227153334
Pubmed

Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic children.

SCN1A SCN2A

1.16e-06238233096315
Pubmed

Electrophysiological Differences between the Same Pore Region Mutation in SCN1A and SCN3A.

SCN1A SCN3A

1.16e-06238224990319
Pubmed

Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series.

SCN1A SCN2A

1.16e-06238231439038
Pubmed

Sodium channel expression within chronic multiple sclerosis plaques.

SCN2A SCN8A

1.16e-06238217805013
Pubmed

Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizures.

SCN1A SCN2A

1.16e-06238226311622
Pubmed

Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy.

SCN1A SCN8A

1.16e-06238233411788
Pubmed

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome.

SCN1A SCN8A

1.16e-06238231943325
Pubmed

Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A.

SCN1A SCN2A

1.16e-06238215249644
Pubmed

Mapping of a FEB3 homologous febrile seizure locus on mouse chromosome 2 containing candidate genes Scn1a and Scn3a.

SCN1A SCN3A

1.16e-06238227690330
Pubmed

The developmental changes of Na(v)1.1 and Na(v)1.2 expression in the human hippocampus and temporal lobe.

SCN1A SCN2A

1.16e-06238221377452
Pubmed

Reduced expression of Na(v)1.6 sodium channels and compensation by Na(v)1.2 channels in mice heterozygous for a null mutation in Scn8a.

SCN2A SCN8A

1.16e-06238218601978
Pubmed

Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome.

SCN1A SCN3A

1.16e-06238223965409
Pubmed

FGF14 N-terminal splice variants differentially modulate Nav1.2 and Nav1.6-encoded sodium channels.

SCN2A SCN8A

1.16e-06238219465131
Pubmed

Persistent Nav1.1 and Nav1.6 currents drive spinal locomotor functions through nonlinear dynamics.

SCN1A SCN8A

1.16e-06238237665666
Pubmed

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.

SCN1A SCN8A

1.16e-06238217881658
Pubmed

SCN1A and SCN2A polymorphisms are associated with response to valproic acid in Chinese epilepsy patients.

SCN1A SCN2A

1.16e-06238230693367
Pubmed

Block of a subset of sodium channels exacerbates experimental autoimmune encephalomyelitis.

SCN2A SCN8A

1.16e-06238223735284
Pubmed

VAPB/ALS8 interacts with FFAT-like proteins including the p97 cofactor FAF1 and the ASNA1 ATPase.

PITPNM1 OSBPL9 WDR44

2.72e-062538324885147
Pubmed

Voltage-gated sodium channels in taste bud cells.

SCN2A SCN3A

3.48e-06338219284629
Pubmed

Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2.

SCN1A SCN2A

3.48e-06338228784306
Pubmed

Association of SCN1A, SCN2A, and UGT2B7 Polymorphisms with Responsiveness to Valproic Acid in the Treatment of Epilepsy.

SCN1A SCN2A

3.48e-06338232185219
Pubmed

Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort.

SCN1A SCN2A

3.48e-06338232005694
Pubmed

Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+).

SCN1A SCN3A

3.48e-06338233895391
Pubmed

Where is the spike generator of the cochlear nerve? Voltage-gated sodium channels in the mouse cochlea.

SCN2A SCN8A

3.48e-06338216033895
Pubmed

Role of sodium channel subtype in action potential generation by neocortical pyramidal neurons.

SCN2A SCN8A

3.48e-06338229991598
Pubmed

GAPDH-mediated posttranscriptional regulations of sodium channel Scn1a and Scn3a genes under seizure and ketogenic diet conditions.

SCN1A SCN3A

3.48e-06338227816501
Pubmed

Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance.

SCN1A SCN8A

3.48e-06338224704313
Pubmed

Gene-to-gene interaction between sodium channel-related genes in determining the risk of antiepileptic drug resistance.

SCN1A SCN2A

3.48e-06338219270815
Pubmed

Identification of functional voltage-gated Na(+) channels in cultured human pulmonary artery smooth muscle cells.

SCN2A SCN3A

3.48e-06338216052353
Pubmed

Association of SCN1A, SCN2A and ABCC2 gene polymorphisms with the response to antiepileptic drugs in Chinese Han patients with epilepsy.

SCN1A SCN2A

3.48e-06338225155934
Pubmed

The sorting receptor Rer1 controls Purkinje cell function via voltage gated sodium channels.

SCN1A SCN8A

3.48e-06338228117367
Pubmed

Experimental and computational evidence that Calpain-10 binds to the carboxy terminus of NaV1.2 and NaV1.6.

SCN2A SCN8A

3.48e-06338238514708
Pubmed

Human Nav1.6 Channels Generate Larger Resurgent Currents than Human Nav1.1 Channels, but the Navβ4 Peptide Does Not Protect Either Isoform from Use-Dependent Reduction.

SCN1A SCN8A

3.48e-06338226182346
Pubmed

De novo SCN1A, SCN8A, and CLCN2 mutations in childhood absence epilepsy.

SCN1A SCN8A

3.48e-06338231054517
Pubmed

Pre-B-cell leukemias in Btk/Slp65-deficient mice arise independently of ongoing V(D)J recombination activity.

BLNK PRKDC

6.96e-06438221030983
Pubmed

Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.

SCN1A SCN2A

6.96e-06438226637798
Pubmed

Models for discovery of targeted therapy in genetic epileptic encephalopathies.

SCN1A SCN8A

6.96e-06438228742937
Pubmed

Interaction between the transcriptional corepressor Sin3B and voltage-gated sodium channels modulates functional channel expression.

SCN2A SCN8A

1.16e-05538224077057
Pubmed

TDP-43 is essential for Eph receptor-class-specific spinal motor axon trajectory into the limb.

FOXP1 MNX1

1.16e-05538234687812
Pubmed

Early development of electrical excitability in the mouse enteric nervous system.

SCN3A SCN8A

1.16e-05538222875929
Pubmed

Are voltage-dependent ion channels involved in the endothelial cell control of vasomotor tone?

SCN2A SCN8A

1.74e-05638217513486
Pubmed

AGR2-Dependent Nuclear Import of RNA Polymerase II Constitutes a Specific Target of Pancreatic Ductal Adenocarcinoma in the Context of Wild-Type p53.

PRKDC PTF1A

1.74e-05638234303658
Pubmed

An animal model of oxaliplatin-induced cold allodynia reveals a crucial role for Nav1.6 in peripheral pain pathways.

SCN3A SCN8A

1.74e-05638223711479
Pubmed

Interrupted Glucagon Signaling Reveals Hepatic α Cell Axis and Role for L-Glutamine in α Cell Proliferation.

FOXP1 PRKDC

1.74e-05638228591638
Pubmed

PDX1 dynamically regulates pancreatic ductal adenocarcinoma initiation and maintenance.

PRKDC PTF1A

2.43e-05738228087712
Pubmed

Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in man.

MNX1 PTF1A

2.43e-05738224411943
Pubmed

Tyrosine-phosphorylated and nonphosphorylated sodium channel beta1 subunits are differentially localized in cardiac myocytes.

SCN1A SCN8A

2.43e-05738215272007
Pubmed

Glucocorticoid signalling affects pancreatic development through both direct and indirect effects.

PRKDC PTF1A

3.24e-05838217001468
Pubmed

Spinal Locomotor Circuits Develop Using Hierarchical Rules Based on Motorneuron Position and Identity.

FOXP1 MNX1

3.24e-05838226335645
Pubmed

Skirting the pitfalls: a clear-cut nomenclature for H3K4 methyltransferases.

KMT2B ASH1L

3.24e-05838223130995
Pubmed

A Gene Regulatory Network Cooperatively Controlled by Pdx1 and Sox9 Governs Lineage Allocation of Foregut Progenitor Cells.

MNX1 PTF1A

4.16e-05938226440894
Pubmed

Sodium channel Scn1b null mice exhibit prolonged QT and RR intervals.

SCN1A SCN8A

4.16e-05938217884088
Pubmed

Foxp1-mediated programming of limb-innervating motor neurons from mouse and human embryonic stem cells.

FOXP1 MNX1

4.16e-05938225868900
Pubmed

A census of human transcription factors: function, expression and evolution.

NPAS3 FOXP1 POU3F3 SP100 MNX1 PTF1A ASH1L

5.03e-0590838719274049
Pubmed

Common variants associated with general and MMR vaccine-related febrile seizures.

SCN1A SCN2A

5.20e-051038225344690
Pubmed

Cux-2 controls the proliferation of neuronal intermediate precursors of the cortical subventricular zone.

FOXP1 POU3F3

5.20e-051038218033766
Pubmed

A retrotransposon insertion in the 5' regulatory domain of Ptf1a results in ectopic gene expression and multiple congenital defects in Danforth's short tail mouse.

MNX1 PTF1A

5.20e-051038223437001
Pubmed

Genetic profile of patients with epilepsy on first-line antiepileptic drugs and potential directions for personalized treatment.

SCN1A SCN2A

5.20e-051038220602612
Pubmed

Vsx1 and Chx10 paralogs sequentially secure V2 interneuron identity during spinal cord development.

FOXP1 MNX1

6.35e-051138231822965
Pubmed

SorCS2 binds progranulin to regulate motor neuron development.

FOXP1 MNX1

6.35e-051138237897724
Pubmed

Dorsal pancreas agenesis in retinoic acid-deficient Raldh2 mutant mice.

MNX1 PTF1A

6.35e-051138216026781
Pubmed

Chx10 Consolidates V2a Interneuron Identity through Two Distinct Gene Repression Modes.

FOXP1 MNX1

6.35e-051138227477290
InteractionSCN4B interactions

SCN1A SCN2A SCN8A

3.44e-078383int:SCN4B
Cytoband2q24.3

SCN1A SCN2A

7.95e-05163822q24.3
CytobandEnsembl 112 genes in cytogenetic band chr2q24

SCN1A SCN2A SCN3A

1.62e-04127383chr2q24
GeneFamilySodium voltage-gated channel alpha subunits

SCN1A SCN2A SCN3A SCN8A

6.69e-1092941203
GeneFamilyPHD finger proteins

SP100 KMT2B ASH1L

3.97e-049029388
GeneFamilyZinc fingers C2H2-type|Lysine methyltransferases|PR/SET domain family

KMT2B ASH1L

1.35e-0334292487
CoexpressionAtlasdev gonad_e13.5_F_MeioticGermCell_Oct_k-means-cluster#1_top-relative-expression-ranked_1000

RAD9B DMXL2 PRKDC SNX25

1.59e-0585384gudmap_dev gonad_e13.5_F_MeioticGermCell_Oct_k1_1000
CoexpressionAtlasB cells, B1a.Sp, IgD+ IgM+ CD45R+ CD24+ CD19+ AA4.1- CD23- CD21/35-, Spleen, avg-3

BLNK ARHGEF12 FOXP1 DMXL2 GBP4 SNX25

2.94e-05341386GSM538225_500
CoexpressionAtlasdev gonad_e13.5_F_MeioticGermCell_Oct_k-means-cluster#3_top-relative-expression-ranked_500

RAD9B DMXL2 PRKDC

4.27e-0538383gudmap_dev gonad_e13.5_F_MeioticGermCell_Oct_k3_500
ToppCellPND03-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

NPAS3 FRMPD3 SCN1A SCN3A STAB1

2.84e-07165385347b59aa625a8a960828b8620824d8ac48990e07
ToppCellPND03-Endothelial-Endothelial_lymphatic|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

NPAS3 FRMPD3 SCN1A SCN3A STAB1

2.84e-071653851890f9c33b0c5b381d57f97042da2610a093a6de
ToppCellPND03-Endothelial-Endothelial_lymphatic-Lymphatic_EC|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

NPAS3 FRMPD3 SCN1A SCN3A STAB1

2.84e-07165385507c89ece0a336b8e9c65b79889a714e17ddca27
ToppCellPND03-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC-LEC_mature|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

NPAS3 FRMPD3 SCN1A SCN3A STAB1

2.84e-0716538539a25be081a5d59c7cf107a997d352793d5025fb
ToppCell10x_3'_v3-tissue-resident_(10x_3'_v3)-lymphocytic-B_lymphocytic-naive_B_cell|tissue-resident_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

BLNK FOXP1 SP100 SCN2A SCN3A

5.71e-07190385a7498fe55b7810c482291db782dc5282675d246a
ToppCellPND01-Immune-Immune_Lymphocytic_T/NK-Lymphocytic_B-B-B_prolif|PND01 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

BLNK SP100 GBP4 FCHO1

1.17e-0516538466f0364098d82629aa2ec1dfe0c5ad23de7c2c12
ToppCellwk_08-11-Mesenchymal-Fibroblast-Alveolar_fibro|wk_08-11 / Celltypes from embryonic and fetal-stage human lung

RAD9B SNX25 WDR44 SCN8A

1.20e-0516638465dafed953b01a9830b54309af75c7a561e88336
ToppCellfacs|World / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

FADS2 SP100 TACC1 KMT2B

1.38e-05172384a2d0a64ebf09d219a07d6bbad1056bad6d46b9be
ToppCellfacs-Trachea-24m-Mesenchymal-myofibroblast-tracheobronchial_smooth_muscle_cell-smooth_muscle_cell_of_trachea_l6-17|24m / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

RAD9B ARMCX4 SCN2A SCN8A

1.54e-051773848abdf1d970b2f15e17e185f3e612dd5065c88757
ToppCellrenal_cortex_nuclei-Adult_normal_reference-Epithelial-Distal_tubule_epithelial_cell-kidney_distal_convoluted_tubule_epithelial_cell-Degenerative_Distal_Convoluted_Tubule_Cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

BLNK POU3F3 SCN2A SCN3A

1.54e-05177384dc846d0feb94d4c289553cc3ac9dac81d10409cb
ToppCellBAL-Control-Myeloid-cDC-cDC-cDC_7|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.09)

FADS2 KMT2B KIF24 STAB1

1.61e-0517938442f3c040f504a91cc69292d39d22b5715c12526f
ToppCellBAL-Control-Myeloid-cDC-cDC-cDC_7|Control / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

FADS2 KMT2B KIF24 STAB1

1.61e-05179384063c05753ef1b4a18bc1ebbcae62c8cd25d11070
ToppCellrenal_papilla_nuclei-Hypertensive_with+without-CKD-Epithelial-Collecting_tubule_epithelial_cell-kidney_collecting_duct_principal_cell-Outer_Medullary_Collecting_Duct_Principal_Cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

BLNK NPAS3 SCN2A SCN3A

1.61e-05179384d3438fed0d85d5ed5afa8ff820c45143d77b6c0d
ToppCellPCW_10-12-Immune_Lymphocytic-Immune_Lymphocytic_B-im_B_cell_(15)|PCW_10-12 / Celltypes from embryonic and fetal-stage human lung

BLNK GBP4 FCHO1 SCN3A

1.68e-0518138451e4d6bfdbf414d8e30aee2e6f7492f4f7f54373
ToppCellEpithelial-lung_neuroendocrine_cell_(PNEC)|World / Lineage, Cell type, age group and donor

NPAS3 SCN2A SCN3A SCN8A

1.72e-0518238457bf4ffb304324e2e392e196336a530d9f78fe0d
ToppCellfacs-Marrow-T-cells-3m-Lymphocytic|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FOXP1 SP100 GBP4

1.79e-05184384b12fb85a064f715a4f0ada1df8e422c359b573cf
ToppCellfacs-Large_Intestine-Proximal-24m-Epithelial-enteroendocrine_cell|Large_Intestine / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

ARMCX4 GBP4 SCN3A SCN8A

1.83e-051853842a8104f610fa5ce618f8105521616722462a0d42
ToppCellfacs-Marrow-T-cells-3m|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FOXP1 SP100 GBP4

1.83e-05185384e1fd0a807def8c2127194108b1a30c6de7024292
ToppCellFetal_29-31_weeks-Epithelial-lung_neuroendocrine_cell_(PNEC)|Fetal_29-31_weeks / Lineage, Cell type, age group and donor

NPAS3 SCN2A SCN3A SCN8A

1.87e-05186384b45cce768e4bf91da194fd9660cab7520dfb15ac
ToppCellSmart-seq2-blood_(Smart-seq2)-lymphocytic-B_lymphocytic-naive_B_cell|blood_(Smart-seq2) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

BLNK FOXP1 SP100 SCN3A

1.91e-05187384160e5f338537d90d50f863a1be801b1071ac7da7
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Epithelial-Distal_tubule_epithelial_cell-kidney_distal_convoluted_tubule_epithelial_cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

BLNK TACC1 SCN2A SCN3A

1.95e-05188384eec3d353e51358db4c7621265ee0fdd4298e5b0e
ToppCellFetal_29-31_weeks-Epithelial-lung_neuroendocrine_cell_(PNEC)-D150|Fetal_29-31_weeks / Lineage, Cell type, age group and donor

NPAS3 SCN2A SCN3A SCN8A

1.95e-05188384c4c3b21ab723b0e9beff9ec84f8d68485f771528
ToppCellrenal_cortex_nuclei-Hypertensive_with+without-CKD-Epithelial-Distal_tubule_epithelial_cell-kidney_distal_convoluted_tubule_epithelial_cell-Distal_Convoluted_Tubule_Cell_Type_1|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

BLNK TACC1 SCN2A SCN3A

1.95e-05188384bc089cd73d283ed7d2ecbb3936673b4edc89f666
ToppCellfacs-Brain_Non-Myeloid-Cerebellum-24m-Neuronal-nan|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

FRMPD3 SCN1A SCN2A SCN8A

1.99e-05189384f57200c93d39c9bce1adba0a6a1c178c028dd86b
ToppCell10x_3'_v3-thymus_(10x_3'_v3)-lymphocytic-B_lymphocytic-naive_B_cell|thymus_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

BLNK SP100 SCN2A SCN3A

1.99e-05189384e2bb5900d210386b7b74938e7a3636d0c7ba1bcf
ToppCell10x_3'_v3-spleen_(10x_3'_v3)-lymphocytic-B_lymphocytic-naive_B_cell|spleen_(10x_3'_v3) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

BLNK FOXP1 SP100 SCN3A

2.08e-05191384b374676ac90572d65895052d46469906e2b6fd93
ToppCellFetal_29-31_weeks-Immune-B_cell|Fetal_29-31_weeks / Lineage, Cell type, age group and donor

BLNK SP100 FCHO1 SCN3A

2.08e-0519138484452125d1b5b76974e3f9126f611eff16d45c25
ToppCellfacs-Marrow-T-cells-3m-Lymphocytic-immature_B_cell|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FOXP1 KIAA0930 SNX25

2.12e-051923842de242d81dc085ae734eb7d1f091af9a542e0866
ToppCellCOVID-19-kidney-CNT|COVID-19 / Disease (COVID-19 only), tissue and cell type

BLNK POU3F3 SCN2A SCN3A

2.12e-05192384760c6b9628de9693034b00c5025c5c4df94bb2e8
ToppCellfacs-Marrow-T-cells-3m-Lymphocytic-immature_B_cell|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FOXP1 KIAA0930 SNX25

2.12e-05192384ba2a683472a8b785dbf666dc6e94356d879486c3
ToppCellfacs-Brain_Non-Myeloid-Cerebellum-24m-Neuronal|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

FRMPD3 SCN1A SCN2A SCN8A

2.16e-051933845fb7808dd971c1cc64c2bd4f8f1de646fb2d77f4
ToppCellPND03-Endothelial-Endothelial_blood-vessel-Microvascular_EC-CAP1|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ARHGEF12 FOXP1 ARMCX4 GBP4

2.21e-0519438444c7d4b75f3b7c9301eba20610e548a01a84ae40
ToppCellPND03-Endothelial-Endothelial_blood-vessel-Microvascular_EC-CAP1-CAP1_mature|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ARHGEF12 FOXP1 ARMCX4 GBP4

2.21e-051943847f24023df47935286f185dd428d48797daf26f49
ToppCellSmart-seq2-bone_marrow_(Smart-seq2)-myeloid|bone_marrow_(Smart-seq2) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

DMXL2 KIAA0930 TNRC18 STAB1

2.25e-05195384b0dbaae86f5703ab62f925e0f36500274044884a
ToppCellCOVID-19-kidney-VWF+PLVAP+VCAM1+EC|kidney / Disease (COVID-19 only), tissue and cell type

TACC1 GBP4 CARD8 STAB1

2.30e-05196384ac2c4a325efa8497a755cd31fb6a9d94d8e3bf42
ToppCellcontrol-B_naive|control / Cohort 1 (10x PBMC) with disease condition, cell group and cell class

BLNK FOXP1 SP100 SCN3A

2.39e-05198384c012b8fbfa8bbc5014217f47acf9177470d8a65a
ToppCellSomatosensory_Cortex_(S1)-Neuronal|Somatosensory_Cortex_(S1) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

SCN1A SCN2A SCN3A SCN8A

2.39e-05198384c01091ef18e096d792ea2a7a715764a5b215355f
ToppCellParenchymal-NucSeq-Epithelial-Epi_airway_neuro-secretory-Neuroendocrine|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

NPAS3 SCN2A SCN3A SCN8A

2.39e-051983848f25e8dff42bad8e779ca618bdb1cb1610667962
ToppCellParenchymal-NucSeq-Epithelial-Epi_airway_neuro-secretory|NucSeq / Cell types per location group and 10X technology with lineage, and cell group designations

NPAS3 SCN2A SCN3A SCN8A

2.39e-05198384e3e0aa3ef20b2370f5b133048510677aaa562dfa
ToppCellprimary_auditory_cortex_(A1C)-Neuronal|primary_auditory_cortex_(A1C) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

SCN1A SCN2A SCN3A SCN8A

2.39e-051983846d18b45eda4014759e6dd282d78ffd28df8a6044
ToppCellPrimary_Motor_Cortex_(M1)-Neuronal|Primary_Motor_Cortex_(M1) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

SCN1A SCN2A SCN3A SCN8A

2.39e-051983844ca5ff320905ab4ff60ed90a5522227c782142a6
ToppCellcontrol-Neutrophil|World / Cohort 1 (10x PBMC) with disease condition, cell group and cell class

DMXL2 KIAA0930 TNRC18 STAB1

2.48e-05200384251ca08fab5cc2a4e280db6a6286a9ebaef3e61a
ToppCellcontrol-Neutrophil|control / Cohort 1 (10x PBMC) with disease condition, cell group and cell class

DMXL2 KIAA0930 TNRC18 STAB1

2.48e-05200384b5d197472799cc61d7497faed91ac2564ae4930a
ToppCellmild-B_naive|World / Cohort 1 (10x PBMC) with disease condition, cell group and cell class

BLNK FOXP1 SP100 SCN3A

2.48e-05200384222789b897e2a683bbfd1d00b6fd8705015d90df
ToppCellcontrol-HLA-DR-_S100A+_Monocyte|control / Cohort 1 (10x PBMC) with disease condition, cell group and cell class

DMXL2 KIAA0930 TNRC18 STAB1

2.48e-052003849e3e13a68bc1110fa000ec2d80f4c654ddbce17e
ToppCellBAL-Control-cDC_7|Control / Compartment, Disease Groups and Clusters

FADS2 KMT2B KIF24

1.49e-04121383b49b044a687a31883dfccecf10a183b5ba567f7a
ToppCellE16.5-samps-Myeloid-Fetal_macrophage-macrophage_-_intermediate_-_unactivated|E16.5-samps / Age Group, Lineage, Cell class and subclass

BLNK SP100 STAB1

2.81e-0415038360fdd266aaca1b589b9a77465a4a7fad4921339a
ToppCellPND07-Immune-Immune_Lymphocytic_T/NK-Lymphocytic_B-B-B_prolif|PND07 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

BLNK SP100 FCHO1

2.81e-04150383cc8361bdcaa16ab6a0d6a3684690d709bc42ff3b
ToppCellPND01-Immune-Immune_Lymphocytic_T/NK-Lymphocytic_B|PND01 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

BLNK SP100 FCHO1

2.87e-04151383ee56b88c56c3b6a5ec9644c43cae521ea0e05920
ToppCellPND01-Immune-Immune_Lymphocytic_T/NK-Lymphocytic_B-B|PND01 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

BLNK SP100 FCHO1

2.87e-041513832c239b09970acbaa90c5ebe1097f453c516f868e
ToppCellSmart-seq2-bone_marrow_(Smart-seq2)-lymphocytic-B_lymphocytic-naive_B_cell|bone_marrow_(Smart-seq2) / Per Platform+tissue_group, by lineage_subgroup, cell_group, cell_type

BLNK SP100 SCN3A

2.87e-041513830f8f07e44c6edaf09574930b416fdce14d67095a
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Epithelial-Distal_tubule_epithelial_cell-kidney_distal_convoluted_tubule_epithelial_cell-Distal_Convoluted_Tubule_Cell_Type_2|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

GCLC SCN1A SCN2A

2.87e-04151383f41c6558a5874b6464c157027fdf202257c60e5b
ToppCellnormal_Lymph_Node-Myeloid_cells-mo-Mac|Myeloid_cells / Location, Cell class and cell subclass

DMXL2 SNX25 STAB1

2.98e-041533835424494ea1f09542799045a875cc3eac13de5079
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

NPAS3 FRMPD3 SNX25

3.10e-04155383e7f49e2fdaf184fa6b4e685518004e7deff1316d
ToppCell10x_3'_v2v3-Non-neoplastic-Glial-Neuronal-OPC-OPC-E|10x_3'_v2v3 / Platform, Oncotype, Lineage, Cell_class, celltype (level4), mutation group

SCN1A SCN2A SCN3A

3.10e-0415538377fdae85d36efb776db977eb424b32487ef222e4
ToppCellrenal_medulla_nuclei-CKD+DKD_normotensive-Epithelial-Renal_corpuscle_epithelial_cell-glomerular_visceral_epithelial_cell-Podocyte|CKD+DKD_normotensive / Celltypes from Cells and Nuclei per compartment and clinical group

NPAS3 FRMPD3 SNX25

3.10e-041553835a872ca70ae8c30b57f45a6772d7bf565e0c2663
ToppCellPND07-Endothelial-Endothelial_lymphatic|PND07 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.46e-04161383133b4fadb499e842c19f573f9cf09ce08c1d4813
ToppCellPND07-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC|PND07 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.46e-04161383cb177ca10d848d0e25399ab5ebfcde1071fb94c2
ToppCellPND07-Endothelial-Endothelial_lymphatic-Lymphatic_EC|PND07 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.46e-041613839466b8658244116f8d21f2f88fb8c2d184b1bdf2
ToppCellrenal_medulla_nuclei-Adult_normal_reference-Epithelial-Collecting_tubule_epithelial_cell-kidney_connecting_tubule_epithelial_cell-Connecting_Tubule_Principal_Cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

BLNK SCN2A SCN3A

3.52e-04162383285e6d553f485fd9f1075c4e1b940da251b5ea35
ToppCellPND07-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC-LEC_mature|PND07 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.52e-0416238396c6e94a10b124a1d25dcd705ec5aaa8609c1089
ToppCellPBMC_fresh-frozen-Mild-Moderate_progression_d12-25-Lymphocytic-Lymphocytic_T-mature_alpha-beta_T_cell-T_CD4_c09-GZMK-FOS_l|Mild-Moderate_progression_d12-25 / Compartment, severity and other cell annotations on 10x 3' data (130k)

TNRC18 ATG2A TRMT61B

3.59e-04163383e4077e587895c85bc806be05ff5d451088e39468
ToppCellLPS-antiTNF-Epithelial_airway-Mes-Epi-like|LPS-antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

KIF24 SCN1A STAB1

3.65e-041643834307b002fb41ddfc7ab8a6bca66a60942c250052
ToppCellPND10-Endothelial-Endothelial_lymphatic-Lymphatic_EC|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.65e-041643837a8e5ef52a8fd2877d59ef0696af8a7af90bbed6
ToppCellrenal_medulla_nuclei-Adult_normal_reference-Epithelial-Collecting_tubule_epithelial_cell-kidney_connecting_tubule_epithelial_cell|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

BLNK SCN2A SCN3A

3.65e-041643836fb2136168f430babfeb81ca7e151ca7a8092ec4
ToppCellPND10-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC-LEC_mature|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.65e-041643835e5bd81414ea2d64f73cdef19a0a78c17bec8c18
ToppCellPND10-Endothelial-Endothelial_lymphatic|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.65e-04164383f13b8d9b7f42193f333d9a77571a1dde6bbb48d8
ToppCellPND10-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC|PND10 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.65e-041643834cfc9f92e49f86d3639e018b35b6a60dc62f494a
ToppCellLPS-antiTNF-Epithelial_airway-Mes-Epi-like-Airway|LPS-antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

KIF24 SCN1A STAB1

3.65e-041643831d84aa5b925f502ee9c5fa39714490f613a58028
ToppCell5'-GW_trimst-2-LargeIntestine-Epithelial-neuro-epithelial-EECs|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

MNX1 GCLC SCN3A

3.72e-041653834b4e75ad0eb0a6b00c30a000ec6267e23ba2e496
ToppCellrenal_papilla_nuclei-Adult_normal_reference-Epithelial-Collecting_tubule_epithelial_cell-kidney_collecting_duct_intercalated_cell-Outer_Medullary_Collecting_Duct_Intercalated_Cell_Type_A|Adult_normal_reference / Celltypes from Cells and Nuclei per compartment and clinical group

FOXP1 SCN2A SCN3A

3.78e-041663836fe8db8d45177a78605681f22e04fa8d0594f2df
ToppCellE16.5-Endothelial-Endothelial_lymphatic|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ARMCX4 SCN3A STAB1

3.85e-04167383b93103a868fba63a8910bffb690a6242b9252833
ToppCellE16.5-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC-LEC_mature|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ARMCX4 SCN3A STAB1

3.85e-0416738326cd8ee5e826e71eaf58d10a906543a6932fb3f9
ToppCellE16.5-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ARMCX4 SCN3A STAB1

3.85e-04167383fcd583b1efd0ac883379982ea8e6c54f2c0be268
ToppCellE16.5-Endothelial-Endothelial_lymphatic-Lymphatic_EC|E16.5 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

ARMCX4 SCN3A STAB1

3.85e-04167383f6bc63138b7239211fa5f27a8dc799b6e022c0f8
ToppCelldroplet-Bladder-BLADDER-1m-Epithelial-basal_bladder_epithelial_cell_(Krt5+Krt14+)|Bladder / Skin_Bladder_Kidney_Mammary_Gland - method, tissue, subtissue, age, lineage, cell ontology and free annotation

KMT2B GCLC KIF24

3.92e-04168383ca65321259711321c175ede67bd67a47aad81d7a
ToppCellPND01-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC-LEC_mature|PND01 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

3.99e-04169383f077e39e41fffe7672541f5b72b80faaf56c597c
ToppCellrenal_medulla_nuclei-Hypertensive_with+without-CKD-Epithelial-Collecting_tubule_epithelial_cell-kidney_connecting_tubule_epithelial_cell-Connecting_Tubule_Cell|Hypertensive_with+without-CKD / Celltypes from Cells and Nuclei per compartment and clinical group

BLNK SCN2A SCN3A

3.99e-041693830332f539a2f7d6dcd081a5d2f567290721f5a329
ToppCellPND01-Endothelial-Endothelial_lymphatic-Lymphatic_EC|PND01 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

4.06e-0417038335e3945d8a540a3e2cec1b559316265aaad023d1
ToppCellControl-Epithelial_cells-ECM-high_epithelial|Control / group, cell type (main and fine annotations)

ARHGEF12 TACC1 SNX25

4.06e-04170383e2023d66e70983c87dacbd6181d3426488d1fc57
ToppCellImmune_cells-Dendritic_cells|World / Lineage and Cell class

BLNK GBP4 SCN3A

4.06e-04170383094dc211d80c89ecb1010855f1fe6eeb71bf0e20
ToppCell10x5'v1-week_17-19-Hematopoietic-HSC/MPP_and_pro-ELP|week_17-19 / cell types per 3 fetal stages;per 3',per 5'

BLNK GBP4 SCN3A

4.06e-04170383a50e558d0b38100ccbdccb90647fe93e85bffd86
ToppCellPND01-Endothelial-Endothelial_lymphatic|PND01 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

4.06e-041703830ea625abaa25bab93b70b7000e8f90d5c0f9a0fb
ToppCellPND01-Endothelial-Endothelial_lymphatic-Lymphatic_EC-LEC|PND01 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

SCN1A SCN3A STAB1

4.06e-041703830b5ddc7d452db0a389927a367914f7d257703f7e
ToppCellfacs|World / Lung_Trachea - method, tissue, subtissue, age, lineage, cell ontology and free annotation

FADS2 SP100 KMT2B

4.13e-041713835bcb96ed7fc15548f2dc9cf47482f890640cb39c
ToppCellfacs|World / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SP100 TACC1 KMT2B

4.13e-04171383c9990bc041a632b2f7bbebbfe737772c423d7027
ToppCellfacs|World / method, tissue, age, lineage, sublineage, cell ontologies, cell type and subtype

FADS2 SP100 KMT2B

4.13e-04171383bb71e816dde44fda6af0ad98d979be9f8740fda6
ToppCelldroplet-Liver-Npc-18m-Lymphocytic-B_cell|Liver / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FOXP1 FCHO1

4.13e-04171383584a095ddcbf78aa29527f84b46b5ad3e2edbaa9
ToppCellfacs-Heart-RV-18m-Lymphocytic-B_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FCHO1 SNX25

4.20e-041723832dcc9d67d6ecc35940eabbc8ed528f5f884f6976
ToppCellPBMC-Mild-Lymphocyte-B-B_cell-B_naive-B_naive-4|Mild / Location, Disease Group, Cell group, Cell class and sub_cluster (2021.03.01)

BLNK FOXP1 SCN3A

4.20e-0417238362ed3b70fa1f6c84ea80ff00f60d2562be292e9d
ToppCellfacs-Heart-RV-18m-Lymphocytic-B_cell|Heart / Tongue_Heart_Limb_Muscle_Aorta_Diaphragm - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FCHO1 SNX25

4.20e-0417238364d2edbd8e2640b76225597883b1a524e6b1dd3b
ToppCelldroplet-Marrow-nan-24m-Hematologic-erythroid_progenitor|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

BLNK FOXP1 SP100

4.20e-04172383910ec7794ea4000db4ef1e2c34e08dbc0243df2c
ToppCellPND03-Immune-Immune_Lymphocytic_T/NK-Lymphocytic_B|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

BLNK SP100 FCHO1

4.20e-041723833784fd1e833703519889942e39fda991f03c3c76
ToppCellPND03-Immune-Immune_Lymphocytic_T/NK-Lymphocytic_B-B|PND03 / Age_group by Lineage, Lineage_subclass, Cell_type, subtypes-by-prolif

BLNK SP100 FCHO1

4.20e-04172383995139aa38f8b9ff23166128b15476cd8a3ff1b8
ToppCell10x5'-lymph-node_spleen-Hematopoietic_progenitors-Cycling_pre-Myeloid-2|lymph-node_spleen / Manually curated celltypes from each tissue

DMXL2 KIAA0930 STAB1

4.27e-04173383783b8fa08b9d8f597f251793eae164151662f1f9
ToppCelldroplet-Large_Intestine-COLON:P+D-30m-Hematologic|Large_Intestine / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SP100 DMXL2 GBP4

4.27e-04173383cd635751f999e12b14c0accfa1c4c1fd3c1d4540
ToppCelldroplet-Large_Intestine-COLON:P+D-30m-Hematologic-hematopoietic_stem_cell|Large_Intestine / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SP100 DMXL2 GBP4

4.27e-041733837456a417c5c1d4ba25f9489065aae322421308a6
ToppCelldroplet-Large_Intestine-COLON:P+D-30m-Hematologic-hematopoietic_stem_cell|Large_Intestine / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SP100 DMXL2 GBP4

4.27e-0417338335586a9e5f15b41609b6224e33eb3aa3cb7e03b7
ToppCellASK452-Immune-B_cell|ASK452 / Donor, Lineage and Cell class of Lung cells from Dropseq

UBL7 RAD9B STAB1

4.34e-0417438369723f5666abc3af5f0431901a60246c9915ef81
ToppCellfacs|World / Fat_BAT_GAT_MAT_SCAT - method, tissue, subtissue, age, lineage, cell ontology and free annotation

FADS2 SP100 KMT2B

4.41e-0417538353e96956019f984decc1c81376ebc88fbf3c4d40
DrugAPETx1, Anthopleura elegantissima

SCN2A SCN3A SCN8A

8.55e-086383ctd:C475726
Drug2,3,5,6-tetrafluoro-4-methylbenzyl (Z)-(1RS)-cis-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate

SCN2A SCN3A SCN8A

2.39e-078383ctd:C489827
DrugZonisamide

SCN1A SCN2A SCN3A

2.87e-0617383DB00909
Drugdecamethrin

GCLC SCN1A SCN2A SCN3A SCN8A

4.28e-06146385ctd:C017180
DrugAPETx2 protein, Anthopleura elegantissima

SCN2A SCN8A

1.62e-054382ctd:C501880
Drugcarmustine; Up 200; 100uM; MCF7; HT_HG-U133A

SIK2 SP100 DMXL2 ATG2A KMT2B

1.79e-051963856888_UP
DrugPilocarpine nitrate [148-72-1]; Down 200; 14.8uM; MCF7; HT_HG-U133A

SIK2 SP100 KMT2B FCHO1 CARD8

1.83e-051973855341_DN
DrugPargyline hydrochloride [306-07-0]; Up 200; 20.4uM; MCF7; HT_HG-U133A

SIK2 SP100 KIAA0930 KMT2B ASH1L

1.93e-051993857016_UP
DrugNatamycin [7681-93-8]; Down 200; 6uM; MCF7; HT_HG-U133A

ARHGEF12 TACC1 KMT2B GCLC FCHO1

1.97e-052003857167_DN
Drugfenpropathrin

SCN2A SCN3A

4.05e-056382ctd:C044267
DrugTetrodotoxin

SCN2A SCN3A SCN8A

4.06e-0540383ctd:D013779
Diseasegeneralized epilepsy with febrile seizures plus 2 (implicated_via_orthology)

SCN1A SCN2A SCN3A SCN8A

4.37e-1010374DOID:0111294 (implicated_via_orthology)
DiseaseDravet syndrome (implicated_via_orthology)

SCN1A SCN2A SCN3A SCN8A

4.37e-1010374DOID:0080422 (implicated_via_orthology)
Diseasegeneralized epilepsy with febrile seizures plus (implicated_via_orthology)

SCN1A SCN2A SCN3A SCN8A

1.03e-0912374DOID:0060170 (implicated_via_orthology)
DiseaseNeurodevelopmental Disorders

FOXP1 SCN1A SCN2A SCN8A ASH1L

1.12e-0793375C1535926
Diseaseanxiety disorder (implicated_via_orthology)

SCN1A SCN2A SCN3A

2.75e-0622373DOID:2030 (implicated_via_orthology)
DiseaseBenign familial infantile epilepsy

SCN2A SCN8A

4.59e-063372cv:C5575231
Diseasecholesteryl ester 14:0 measurement

FADS2 CARD8 SCN3A

5.20e-0627373EFO_0010340
DiseaseFamilial benign neonatal epilepsy

SCN2A SCN8A

2.29e-056372C0220669
DiseaseBipolar Disorder

NPAS3 FADS2 PLA2G4A SCN2A SCN8A STAB1

2.63e-05477376C0005586
DiseaseSeizure, Febrile, Simple

SCN1A SCN2A

3.20e-057372C0149886
DiseaseSeizure, Febrile, Complex

SCN1A SCN2A

3.20e-057372C0751057
Diseaseepilepsy (implicated_via_orthology)

SCN1A SCN2A SCN3A SCN8A

5.14e-05163374DOID:1826 (implicated_via_orthology)
DiseaseFebrile Convulsions

SCN1A SCN2A

5.48e-059372C0009952
DiseaseGeneralized Epilepsy with Febrile Seizures Plus

SCN1A SCN2A

5.48e-059372C3502809
DiseaseInfantile Severe Myoclonic Epilepsy

SCN1A SCN2A

1.18e-0413372C0751122
DiseaseManic

FADS2 SCN2A STAB1

1.29e-0478373C0338831
DiseaseEpilepsy, Cryptogenic

SCN1A SCN2A SCN8A

1.50e-0482373C0086237
DiseaseAwakening Epilepsy

SCN1A SCN2A SCN8A

1.50e-0482373C0751111
DiseaseAura

SCN1A SCN2A SCN8A

1.50e-0482373C0236018
DiseaseMMR-related febrile seizures

SCN1A SCN2A

1.59e-0415372EFO_0006519
DiseaseEarly infantile epileptic encephalopathy with suppression bursts

SCN1A SCN2A

1.82e-0416372C0393706
DiseaseIntellectual Disability

POU3F3 SCN1A SCN3A SCN8A ASH1L

2.28e-04447375C3714756
DiseaseFebrile seizure (within the age range of 3 months to 6 years)

SCN1A SCN2A

2.31e-0418372HP_0002373
Diseaseeosinophil percentage of leukocytes

UBL7 SIK2 FADS2 FOXP1 PRKDC KMT2B

3.05e-04746376EFO_0007991
Diseasegestational age, birth measurement

NPAS3 FADS2

3.16e-0421372EFO_0005112, EFO_0006921
DiseaseEpilepsy

SCN1A SCN2A SCN8A

3.48e-04109373C0014544
Diseasecortical thickness

ARHGEF12 FADS2 FOXP1 POU3F3 TACC1 KMT2B STAB1

4.07e-041113377EFO_0004840
DiseaseNeonatal diabetes mellitus

MNX1 PTF1A

4.51e-0425372C0158981
Diseaseautism spectrum disorder (implicated_via_orthology)

SCN1A SCN2A ASH1L

9.16e-04152373DOID:0060041 (implicated_via_orthology)
Diseaseskin microbiome measurement

NPAS3 CARD8

1.10e-0339372EFO_0801228
Diseaseepilepsy

PLA2G4A SCN1A

1.22e-0341372EFO_0000474
Diseaseexecutive function measurement

NPAS3 DMXL2 CARD8 STAB1

1.23e-03376374EFO_0009332

Protein segments in the cluster

PeptideGeneStartEntry
SEGSYHFDPDNFDES

TACC1

411

O75410
SDNHRSSSDFFESED

ASH1L

926

Q9NR48
IHSDEEDDAFFSDTQ

DMXL2

2481

Q8TDJ6
FAHQSEASFPVEDES

ARMCX4

2001

Q5H9R4
DSDSDDEDAHFFSVG

ATG2A

891

Q2TAZ0
FFDAREAHSDENPSE

ARHGEF12

1381

Q9NZN5
GTSDADLFDSHDDRD

OSBPL9

346

Q96SU4
HPFDSLARASDSEED

RAD9B

391

Q6WBX8
EDATDAFRAFHPDLE

FADS2

66

O95864
RFSSSDSDFDDEEPR

FCHO1

341

O14526
DEDDEDHFPYSNGAS

MNX1

361

P50219
KSHSANDSEEFFRED

KIAA0930

321

Q6ICG6
NHSPDFDHDRDYEDE

FOXP1

656

Q9H334
FTEDDEASRASKPDH

GCLC

221

P48506
EELDDSDFSEDSFSH

KIF24

821

Q5T7B8
DEAEDSSEFASFFPD

GBP4

176

Q96PP9
EEFQGFHSDEDVAPS

KMT2B

121

Q9UMN6
FDEDDFFTDQSSRDP

PTF1A

21

Q7RTS3
DDFDSDYENPDEHSD

BLNK

66

Q8WV28
DDFDAASLDHEPCAS

FRMPD3

611

Q5JV73
SHFFQEDDETEAEPL

CARD8

86

Q9Y2G2
HSDEDTPTSDDLEQF

POU3F3

311

P20264
PLSDFATQDSFDDDE

PLA2G4A

506

P47712
RDFFSHQEEETEEDS

SNX25

651

Q9H3E2
EAEEDPAHAFEAFQS

SIK2

461

Q9H0K1
SNPDSRDSDDSFEHS

NPAS3

521

Q8IXF0
RDSDDSFEHSDFENP

NPAS3

526

Q8IXF0
NDFADDEHSTFEDSE

SCN3A

591

Q9NY46
SENDFADDEHSTFED

SCN1A

586

P35498
ADDEHSTFEDNESRR

SCN1A

591

P35498
DSENSSEEEFFDAHE

PITPNM1

341

O00562
FEPNQDSSFSEDEHL

TNRC18

2121

O15417
LFQEDDHEESHSDFP

TRMT61B

431

Q9BVS5
GQDHDFSESSEEEAP

SP100

401

P23497
DEHSTFEDNDSRRDS

SCN2A

596

Q99250
FEGLSDDEDDFHPNT

UBL7

226

Q96S82
VFHTDQDDPSSSDDE

WDR44

461

Q5JSH3
DPGSENEFADDEHST

SCN8A

576

Q9UQD0
SAFQAEDDADDDFSP

STAB1

2511

Q9NY15
HDNYRDPESETDNDS

PRKDC

2481

P78527