Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionsodium ion binding

ATP1A2 SCN1A SCN8A SCN9A

4.10e-0914304GO:0031402
GeneOntologyMolecularFunctionalkali metal ion binding

ATP1A2 SCN1A SCN8A SCN9A

6.05e-0826304GO:0031420
GeneOntologyMolecularFunctionvoltage-gated sodium channel activity

SCN1A SCN8A SCN9A

7.77e-0626303GO:0005248
GeneOntologyMolecularFunctioninorganic cation transmembrane transporter activity

SLC30A7 HRH1 SLC45A2 ATP1A2 SCN1A SCN8A SCN9A

3.16e-05627307GO:0022890
GeneOntologyMolecularFunctiontransmembrane transporter activity

SLC30A7 HRH1 SLC45A2 SLC7A3 ATP1A2 SLC16A2 SCN1A SCN8A SCN9A

3.94e-051180309GO:0022857
GeneOntologyMolecularFunctionmonoatomic cation transmembrane transporter activity

SLC30A7 HRH1 SLC45A2 ATP1A2 SCN1A SCN8A SCN9A

4.55e-05664307GO:0008324
GeneOntologyMolecularFunctionmetal ion transmembrane transporter activity

SLC30A7 HRH1 ATP1A2 SCN1A SCN8A SCN9A

5.70e-05465306GO:0046873
GeneOntologyMolecularFunctionsodium channel activity

SCN1A SCN8A SCN9A

6.44e-0552303GO:0005272
GeneOntologyMolecularFunctiontransporter activity

SLC30A7 HRH1 SLC45A2 SLC7A3 ATP1A2 SLC16A2 SCN1A SCN8A SCN9A

7.85e-051289309GO:0005215
GeneOntologyMolecularFunctioninorganic molecular entity transmembrane transporter activity

SLC30A7 HRH1 SLC45A2 ATP1A2 SCN1A SCN8A SCN9A

1.05e-04758307GO:0015318
GeneOntologyMolecularFunctionsodium ion transmembrane transporter activity

ATP1A2 SCN1A SCN8A SCN9A

1.20e-04171304GO:0015081
GeneOntologyMolecularFunctionmonoatomic ion transmembrane transporter activity

SLC30A7 HRH1 SLC45A2 ATP1A2 SCN1A SCN8A SCN9A

1.39e-04793307GO:0015075
GeneOntologyMolecularFunctionodorant binding

OR8K3 OR5M3 OR5AP2

9.00e-04127303GO:0005549
GeneOntologyMolecularFunctionolfactory receptor activity

OR8K3 OR5M3 OR2T6 OR5AP2

3.76e-03431304GO:0004984
GeneOntologyMolecularFunctionG protein-coupled receptor activity

HRH1 OR8K3 OR5M3 OR2T6 OR5AP2

9.54e-03884305GO:0004930
GeneOntologyMolecularFunctionamino acid transmembrane transporter activity

SLC7A3 SLC16A2

1.08e-02105302GO:0015171
GeneOntologyBiologicalProcessmembrane depolarization during action potential

ATP1A2 SCN1A SCN8A SCN9A

1.80e-0736294GO:0086010
GeneOntologyBiologicalProcesscardiac muscle cell action potential

ATP1A2 SCN1A SCN8A SCN9A

6.47e-0687294GO:0086001
GeneOntologyBiologicalProcesscardiac muscle cell contraction

ATP1A2 SCN1A SCN8A SCN9A

8.44e-0693294GO:0086003
GeneOntologyBiologicalProcesstransmission of nerve impulse

ATP1A2 SCN1A SCN8A SCN9A

1.76e-05112294GO:0019226
GeneOntologyBiologicalProcessmembrane depolarization

ATP1A2 SCN1A SCN8A SCN9A

2.39e-05121294GO:0051899
GeneOntologyBiologicalProcessactin-mediated cell contraction

ATP1A2 SCN1A SCN8A SCN9A

2.89e-05127294GO:0070252
GeneOntologyBiologicalProcesscirculatory system process

HRH1 SLC7A3 ATP1A2 SLC16A2 SCN1A SCN8A SCN9A

5.48e-05733297GO:0003013
GeneOntologyBiologicalProcessactin filament-based movement

ATP1A2 SCN1A SCN8A SCN9A

5.98e-05153294GO:0030048
GeneOntologyBiologicalProcessamino acid import across plasma membrane

SLC7A3 ATP1A2 SLC16A2

7.32e-0558293GO:0089718
GeneOntologyBiologicalProcesssensory perception

SLC45A2 OR8K3 OR5M3 OR2T6 SCN1A OR5AP2 SCN8A SCN9A

8.36e-051072298GO:0007600
GeneOntologyBiologicalProcesscardiac muscle contraction

ATP1A2 SCN1A SCN8A SCN9A

8.41e-05167294GO:0060048
GeneOntologyBiologicalProcesscardiac muscle cell action potential involved in contraction

SCN1A SCN8A SCN9A

8.94e-0562293GO:0086002
GeneOntologyBiologicalProcessneuronal action potential

SCN1A SCN8A SCN9A

9.38e-0563293GO:0019228
GeneOntologyBiologicalProcessneuronal action potential propagation

ATP1A2 SCN1A

1.25e-0412292GO:0019227
GeneOntologyBiologicalProcessaction potential propagation

ATP1A2 SCN1A

1.25e-0412292GO:0098870
GeneOntologyBiologicalProcessdetection of stimulus involved in sensory perception

OR8K3 OR5M3 OR2T6 SCN1A OR5AP2 SCN9A

1.34e-04582296GO:0050906
GeneOntologyBiologicalProcessaction potential

ATP1A2 SCN1A SCN8A SCN9A

1.72e-04201294GO:0001508
GeneOntologyBiologicalProcesssodium ion transmembrane transport

ATP1A2 SCN1A SCN8A SCN9A

1.96e-04208294GO:0035725
GeneOntologyBiologicalProcessstriated muscle contraction

ATP1A2 SCN1A SCN8A SCN9A

2.30e-04217294GO:0006941
GeneOntologyBiologicalProcesstransport across blood-brain barrier

SLC7A3 ATP1A2 SLC16A2

2.45e-0487293GO:0150104
GeneOntologyBiologicalProcessvascular transport

SLC7A3 ATP1A2 SLC16A2

2.53e-0488293GO:0010232
GeneOntologyBiologicalProcessdetection of stimulus

OR8K3 OR5M3 OR2T6 SCN1A OR5AP2 SCN9A

4.30e-04722296GO:0051606
GeneOntologyBiologicalProcesssodium ion transport

ATP1A2 SCN1A SCN8A SCN9A

5.65e-04275294GO:0006814
GeneOntologyBiologicalProcessadult locomotory behavior

ATP1A2 SCN1A SCN8A

5.69e-04116293GO:0008344
GeneOntologyBiologicalProcessamino acid transmembrane transport

SLC7A3 ATP1A2 SLC16A2

6.28e-04120293GO:0003333
GeneOntologyBiologicalProcessheart contraction

ATP1A2 SCN1A SCN8A SCN9A

7.63e-04298294GO:0060047
GeneOntologyBiologicalProcessheart process

ATP1A2 SCN1A SCN8A SCN9A

8.73e-04309294GO:0003015
GeneOntologyBiologicalProcessvascular process in circulatory system

HRH1 SLC7A3 ATP1A2 SLC16A2

1.30e-03344294GO:0003018
GeneOntologyBiologicalProcessinorganic cation transmembrane transport

SLC30A7 HRH1 ATP1A2 SCN1A SCN8A SCN9A

1.54e-03922296GO:0098662
GeneOntologyCellularComponentvoltage-gated sodium channel complex

SCN1A SCN8A SCN9A

1.79e-0617303GO:0001518
GeneOntologyCellularComponentsodium channel complex

SCN1A SCN8A SCN9A

9.50e-0629303GO:0034706
GeneOntologyCellularComponentnode of Ranvier

SCN1A SCN8A

3.72e-0420302GO:0033268
GeneOntologyCellularComponentaxon initial segment

SCN1A SCN8A

7.89e-0429302GO:0043194
HumanPhenoComplex febrile seizure

ATP1A2 SCN1A SCN8A SCN9A

2.12e-0816114HP:0011172
HumanPhenoAbnormal facial expression

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A SCN9A

8.41e-07185116HP:0005346
HumanPhenoFocal automatism seizure

ATP1A2 SCN1A SCN8A

1.63e-0612113HP:0032898
HumanPhenoChoreoathetosis

ATM ATP1A2 SLC16A2 SCN1A SCN8A

3.11e-06123115HP:0001266
HumanPhenoFacial tics

ATP1A2 SCN1A SCN9A

3.36e-0615113HP:0011468
HumanPhenoFocal sensory seizure

ATP1A2 SCN1A SCN8A

1.13e-0522113HP:0011157
HumanPhenoAthetosis

ATM ATP1A2 SLC16A2 SCN1A SCN8A

1.36e-05166115HP:0002305
HumanPhenoFocal hemiclonic seizure

SCN1A SCN8A SCN9A

1.68e-0525113HP:0006813
HumanPhenoEpileptic aura

ATP1A2 SCN1A SCN8A

1.68e-0525113HP:0033348
HumanPhenoClonic seizure

ATP1A2 SCN1A SCN8A SCN9A

1.80e-0581114HP:0020221
HumanPhenoAlien limb phenomenon

ATP1A2 SCN1A

2.54e-054112HP:0032506
HumanPhenoFocal manual automatism seizure

ATP1A2 SCN1A

2.54e-054112HP:0032900
HumanPhenoFocal pedal automatism seizure

ATP1A2 SCN1A

2.54e-054112HP:0032901
HumanPhenoDissociated sensory loss

ATP1A2 SCN1A

2.54e-054112HP:0010835
HumanPhenoProgressive gait ataxia

ATP1A2 SCN1A SCN9A

2.95e-0530113HP:0007240
HumanPhenoProgressive ataxia

ATP1A2 SCN1A SCN9A

2.95e-0530113HP:0001329
HumanPhenoSeesaw nystagmus

ATP1A2 SCN1A

4.22e-055112HP:0012044
HumanPhenoSpontaneous pain sensation

ATP1A2 SCN1A

4.22e-055112HP:0010833
HumanPhenoGeneralized clonic seizure

SCN1A SCN8A SCN9A

4.32e-0534113HP:0011169
HumanPhenoAbnormality of temperature sensation

ATP1A2 SCN1A SCN9A

4.32e-0534113HP:0100772
HumanPhenoImpaired temperature sensation

ATP1A2 SCN1A SCN9A

4.32e-0534113HP:0010829
HumanPhenoLimitation of neck motion

ATP1A2 SCN1A SCN9A

5.15e-0536113HP:0005986
HumanPhenoDisturbance of facial expression

ATP1A2 SCN1A SCN9A

5.15e-0536113HP:0005324
HumanPhenoAbnormal neck physiology

ATP1A2 SCN1A SCN9A

5.15e-0536113HP:0025669
HumanPhenoFacial palsy

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A

6.92e-05232115HP:0010628
HumanPhenoAbnormal seventh cranial physiology

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A

7.07e-05233115HP:0010827
HumanPhenoFocal non-motor seizure

ATP1A2 SCN1A SCN8A

7.09e-0540113HP:0032679
HumanPhenoAmaurosis fugax

ATM ATP1A2 SCN1A

7.64e-0541113HP:0100576
HumanPhenoEEG with focal epileptiform discharges

ATP1A2 SCN1A SCN8A SCN9A

7.96e-05118114HP:0011185
HumanPhenoFocal clonic seizure

SCN1A SCN8A SCN9A

8.22e-0542113HP:0002266
HumanPhenoChorea

ATM ATP1A2 SLC16A2 SCN1A SCN8A

9.53e-05248115HP:0002072
HumanPhenoFirst dorsal interossei muscle weakness

ATP1A2 SCN1A

1.18e-048112HP:0003392
HumanPhenoPhotosensitive myoclonic seizure

SCN1A SCN9A

1.18e-048112HP:0001327
HumanPhenoCyanotic episode

SCN1A SCN9A

1.18e-048112HP:0200048
HumanPhenoFocal motor seizure

ATP1A2 SCN1A SCN8A SCN9A

1.20e-04131114HP:0011153
HumanPhenoWeakness of facial musculature

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A

1.41e-04269115HP:0030319
HumanPhenoBilateral tonic-clonic seizure with focal onset

ATP1A2 SCN1A SCN8A

1.56e-0452113HP:0007334
HumanPhenoParesthesia

ATM ATP1A2 SCN1A SCN9A

1.73e-04144114HP:0003401
HumanPhenoInfection-related seizure

ATP1A2 SCN1A SCN8A SCN9A

1.78e-04145114HP:0032892
HumanPhenoSeizure precipitated by febrile infection

ATP1A2 SCN1A SCN8A SCN9A

1.78e-04145114HP:0032894
HumanPhenoFebrile seizure (within the age range of 3 months to 6 years)

ATP1A2 SCN1A SCN8A SCN9A

1.78e-04145114HP:0002373
HumanPhenoGaze-evoked nystagmus

ATP1A2 SCN1A SCN8A

1.85e-0455113HP:0000640
HumanPhenoEEG with generalized sharp slow waves

ATP1A2 SCN1A

1.89e-0410112HP:0011199
HumanPhenoDecreased vigilance

ATP1A2 SCN1A

1.89e-0410112HP:0032044
HumanPhenoSudden unexpected death in epilepsy

SCN1A SCN8A

1.89e-0410112HP:0033258
HumanPhenoPes valgus

SLC16A2 SCN1A SCN9A

1.95e-0456113HP:0008081
HumanPhenoImpulsivity

ATP1A2 SCN1A SCN8A SCN9A

1.98e-04149114HP:0100710
HumanPhenoMyopathic facies

SLC16A2 PYROXD1 TNPO2

2.06e-0457113HP:0002058
HumanPhenoLimited neck range of motion

SCN1A SCN9A

2.31e-0411112HP:0000466
HumanPhenoFacial paralysis

ATP1A2 SCN1A

2.31e-0411112HP:0007209
HumanPhenoEEG with focal sharp waves

ATP1A2 SCN1A

2.77e-0412112HP:0011196
HumanPhenoMigraine with aura

ATP1A2 SCN1A

2.77e-0412112HP:0002077
HumanPhenoEpilepsia partialis continua

SCN1A SCN9A

2.77e-0412112HP:0012847
HumanPhenoNuchal rigidity

ATP1A2 SCN1A

2.77e-0412112HP:0031179
HumanPhenoGeneralized tonic seizure

SCN1A SCN8A SCN9A

2.91e-0464113HP:0010818
HumanPhenoShort attention span

ATM ATP1A2 TNPO2 SCN1A SCN8A SCN9A

3.14e-04517116HP:0000736
HumanPhenoMultifocal epileptiform discharges

SCN1A SCN8A SCN9A

3.18e-0466113HP:0010841
HumanPhenoGeneralized cerebral atrophy/hypoplasia

SCN1A SCN9A

3.26e-0413112HP:0007058
HumanPhenoReduced attention regulation

ATM ATP1A2 TNPO2 SCN1A SCN8A SCN9A

3.46e-04526116HP:5200044
HumanPhenoCranial nerve paralysis

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A

3.64e-04329115HP:0006824
HumanPhenoAbnormal cranial nerve physiology

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A

3.80e-04332115HP:0031910
HumanPhenoPhotosensitive tonic-clonic seizure

SCN1A SCN9A

4.38e-0415112HP:0007207
HumanPhenoDysgenesis of the hippocampus

SCN1A SCN9A

5.00e-0416112HP:0025101
HumanPhenoParoxysmal dyskinesia

ATP1A2 SCN8A

5.00e-0416112HP:0007166
HumanPhenoAbnormal oral physiology

ATP1A2 SLC16A2 PYROXD1 SCN1A SCN9A

5.20e-04355115HP:0031815
HumanPhenoAbnormality of facial musculature

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A

5.62e-04361115HP:0000301
HumanPhenoAtypical absence status epilepticus

SCN1A SCN9A

5.67e-0417112HP:0011151
HumanPhenoFocal motor status epilepticus

SCN1A SCN9A

5.67e-0417112HP:0032663
HumanPhenoNon-motor seizure

ATP1A2 SCN1A SCN8A SCN9A

5.78e-04197114HP:0033259
HumanPhenoDyskinesia

ATM ATP1A2 SLC16A2 SCN8A

5.89e-04198114HP:0100660
HumanPhenoPes planus

ATP1A2 SLC16A2 PYROXD1 SCN1A SCN9A

5.92e-04365115HP:0001763
HumanPhenoGaze-evoked horizontal nystagmus

ATP1A2 SCN1A

6.37e-0418112HP:0007979
HumanPhenoVisually-induced seizure

SCN1A SCN9A

6.37e-0418112HP:0020216
HumanPhenoGeneralized non-convulsive status epilepticus without coma

SCN1A SCN9A

6.37e-0418112HP:0032860
HumanPhenoMyoclonus

ATM ATP1A2 SCN1A SCN8A SCN9A

6.38e-04371115HP:0001336
HumanPhenoAbnormal cranial nerve morphology

ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A

6.71e-04375115HP:0001291
HumanPhenoIncoordination

ATM ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A SCN8A SCN9A

6.94e-041184118HP:0002311
HumanPhenoStatus epilepticus

ATP1A2 SCN1A SCN8A SCN9A

6.98e-04207114HP:0002133
HumanPhenoCSF lymphocytic pleiocytosis

ATP1A2 SCN1A

7.11e-0419112HP:0200149
HumanPhenoEEG with spike-wave complexes

SCN1A SCN8A SCN9A

7.44e-0488113HP:0010850
HumanPhenoEEG with abnormally slow frequencies

ATP1A2 SCN1A SCN8A

7.44e-0488113HP:0011203
HumanPhenoNon-convulsive status epilepticus without coma

SCN1A SCN9A

7.89e-0420112HP:0032671
HumanPhenoRigidity

ATP1A2 SCN1A SCN8A SCN9A

7.92e-04214114HP:0002063
HumanPhenoAbnormal myelination

ATP1A2 SLC16A2 TNPO2 SCN1A SCN8A SCN9A

8.69e-04622116HP:0012447
HumanPhenoTalipes valgus

SCN1A SCN9A

8.71e-0421112HP:0004684
HumanPhenoAbnormality of coordination

ATM ATP1A2 SLC16A2 PYROXD1 TNPO2 SCN1A SCN8A SCN9A

8.98e-041227118HP:0011443
HumanPhenoReflex seizure

SCN1A SCN9A

9.57e-0422112HP:0020207
HumanPhenoGeneralized-onset motor seizure

ATP1A2 SCN1A SCN8A SCN9A

1.01e-03228114HP:0032677
HumanPhenoTremor

ATM ATP1A2 TNPO2 SCN1A SCN8A SCN9A

1.01e-03639116HP:0001337
HumanPhenoTibial torsion

SCN1A SCN9A

1.05e-0323112HP:0100694
HumanPhenoVertical nystagmus

ATP1A2 SCN1A

1.05e-0323112HP:0010544
HumanPhenoAttention deficit hyperactivity disorder

ATM ATP1A2 TNPO2 SCN1A SCN8A

1.05e-03413115HP:0007018
HumanPhenoPallor

SLC45A2 ATM ATP1A2 SCN1A SCN9A

1.09e-03417115HP:0000980
HumanPhenoMask-like facies

SLC16A2 PYROXD1 TNPO2

1.39e-03109113HP:0000298
HumanPhenoIntellectual disability, profound

SLC16A2 SCN1A SCN8A

1.39e-03109113HP:0002187
HumanPhenoDevelopmental regression

ATM ATP1A2 SCN1A SCN8A SCN9A

1.40e-03440115HP:0002376
HumanPhenoSimple febrile seizure

SCN1A SCN8A

1.44e-0327112HP:0011171
HumanPhenoCSF pleocytosis

ATP1A2 SCN1A

1.44e-0327112HP:0012229
HumanPhenoLimited knee extension

SCN1A SCN9A

1.44e-0327112HP:0003066
HumanPhenoStatus epilepticus without prominent motor symptoms

SCN1A SCN9A

1.44e-0327112HP:0031475
MousePhenoabnormal action potential

ATP1A2 SCN1A SCN8A SCN9A

3.37e-05133204MP:0005402
DomainNa_trans_cytopl

SCN1A SCN8A SCN9A

6.71e-086293PF11933
DomainNa_trans_cytopl

SCN1A SCN8A SCN9A

6.71e-086293IPR024583
DomainNa_channel_asu

SCN1A SCN8A SCN9A

4.01e-0710293IPR001696
DomainNa_trans_assoc

SCN1A SCN8A SCN9A

4.01e-0710293IPR010526
DomainNa_trans_assoc

SCN1A SCN8A SCN9A

4.01e-0710293PF06512
DomainChannel_four-helix_dom

SCN1A SCN8A SCN9A

9.31e-0557293IPR027359
Domain-

SCN1A SCN8A SCN9A

9.31e-05572931.20.120.350
DomainIQ

SCN1A SCN8A SCN9A

1.79e-0471293PF00612
DomainIQ

SCN1A SCN8A SCN9A

2.65e-0481293SM00015
DomainIQ_motif_EF-hand-BS

SCN1A SCN8A SCN9A

3.61e-0490293IPR000048
DomainIQ

SCN1A SCN8A SCN9A

3.98e-0493293PS50096
DomainIon_trans_dom

SCN1A SCN8A SCN9A

7.21e-04114293IPR005821
DomainIon_trans

SCN1A SCN8A SCN9A

7.21e-04114293PF00520
DomainARM-type_fold

RIC8B ATM ARMC2 TNPO2

1.77e-03339294IPR016024
DomainArmadillo

ARMC2 TNPO2

2.41e-0347292IPR000225
DomainOlfact_rcpt

OR8K3 OR5M3 OR2T6 OR5AP2

3.02e-03393294IPR000725
DomainGPCR_Rhodpsn_7TM

HRH1 OR8K3 OR5M3 OR2T6 OR5AP2

3.40e-03670295IPR017452
Domain7tm_1

HRH1 OR8K3 OR5M3 OR2T6 OR5AP2

3.55e-03677295PF00001
DomainG_PROTEIN_RECEP_F1_1

HRH1 OR8K3 OR5M3 OR2T6 OR5AP2

3.74e-03685295PS00237
DomainG_PROTEIN_RECEP_F1_2

HRH1 OR8K3 OR5M3 OR2T6 OR5AP2

3.88e-03691295PS50262
DomainGPCR_Rhodpsn

HRH1 OR8K3 OR5M3 OR2T6 OR5AP2

3.90e-03692295IPR000276
Domain-

RIC8B ARMC2 TNPO2

4.82e-032222931.25.10.10
DomainMFS

SLC45A2 SLC16A2

6.34e-0377292IPR011701
DomainMFS_1

SLC45A2 SLC16A2

6.34e-0377292PF07690
DomainARM-like

RIC8B ARMC2 TNPO2

8.27e-03270293IPR011989
DomainEF-hand-dom_pair

SCN1A SCN8A SCN9A

9.77e-03287293IPR011992
DomainMFS_dom

SLC45A2 SLC16A2

1.83e-02134292IPR020846
PathwayREACTOME_INTERACTION_BETWEEN_L1_AND_ANKYRINS

SCN1A SCN8A SCN9A

1.07e-0531203M877
PathwayREACTOME_PHASE_0_RAPID_DEPOLARISATION

SCN1A SCN8A SCN9A

1.18e-0532203M27455
PathwayREACTOME_CARDIAC_CONDUCTION

ATP1A2 SCN1A SCN8A SCN9A

2.98e-05130204M27454
PathwayREACTOME_MUSCLE_CONTRACTION

ATP1A2 SCN1A SCN8A SCN9A

1.69e-04203204M5485
PathwayREACTOME_L1CAM_INTERACTIONS

SCN1A SCN8A SCN9A

6.32e-04121203M872
PathwayWP_DRAVET_SYNDROME

SCN1A SCN8A

7.07e-0428202M45519
Pubmed

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

SCN1A SCN8A SCN9A

1.16e-08630323652591
Pubmed

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

SCN1A SCN8A SCN9A

4.85e-08930316382098
Pubmed

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

SCN1A SCN8A SCN9A

1.65e-071330315123669
Pubmed

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

SCN1A SCN8A

7.19e-07230237901435
Pubmed

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

SCN1A SCN8A

7.19e-07230233411788
Pubmed

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

SCN1A SCN8A

7.19e-07230226410685
Pubmed

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

SCN1A SCN8A

7.19e-07230231943325
Pubmed

Sodium channel slow inactivation interferes with open channel block.

SCN8A SCN9A

7.19e-07230227174182
Pubmed

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

SCN1A SCN8A

7.19e-07230237665666
Pubmed

Genetics of migraine: an update with special attention to genetic comorbidity.

ATP1A2 SCN1A

7.19e-07230218451712
Pubmed

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

SCN1A SCN8A

7.19e-07230217881658
Pubmed

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

SCN1A SCN8A

2.16e-06330224704313
Pubmed

Familial Hemiplegic Migraine

ATP1A2 SCN1A

2.16e-06330220301562
Pubmed

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine.

ATP1A2 SCN1A

2.16e-06330218056581
Pubmed

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

SCN1A SCN8A

2.16e-06330228117367
Pubmed

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

SCN1A SCN9A

2.16e-06330233895391
Pubmed

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

SCN1A SCN8A

2.16e-06330217928448
Pubmed

The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families.

ATP1A2 SCN1A

2.16e-06330229486580
Pubmed

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

CAPN10 SCN8A

2.16e-06330238514708
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

2.16e-06330226182346
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 SCN8A

2.16e-06330232845893
Pubmed

FHM3 in familial hemiplegic migraine is more resistant to mutation than FHM1 and FHM2.

ATP1A2 SCN1A

2.16e-06330219007941
Pubmed

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

SCN1A SCN8A

2.16e-06330231054517
Pubmed

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

SCN1A SCN8A

2.16e-06330228518218
Pubmed

Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine.

ATP1A2 SCN1A

2.16e-06330231980564
Pubmed

Expression of alternatively spliced sodium channel alpha-subunit genes. Unique splicing patterns are observed in dorsal root ganglia.

SCN8A SCN9A

2.16e-06330215302875
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 SCN8A

4.31e-06430217537961
Pubmed

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

SCN1A SCN8A

4.31e-06430235031483
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 SCN8A

4.31e-06430229578003
Pubmed

Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes.

ATP1A2 SCN1A

4.31e-06430226747084
Pubmed

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

SCN1A SCN8A

4.31e-06430221156207
Pubmed

Models for discovery of targeted therapy in genetic epileptic encephalopathies.

SCN1A SCN8A

4.31e-06430228742937
Pubmed

Dorsal root ganglia isolated from Nf1+/- mice exhibit increased levels of mRNA expression of voltage-dependent sodium channels.

SCN1A SCN9A

4.31e-06430222260870
Pubmed

Large-scale analysis of ion channel gene expression in the mouse heart during perinatal development.

ATP1A2 SCN1A SCN8A SCN9A

6.18e-0613930416985003
Pubmed

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

SCN1A SCN9A

7.18e-0653028812438
Pubmed

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

SCN8A SCN9A

7.18e-06530222875929
Pubmed

Contactin regulates the current density and axonal expression of tetrodotoxin-resistant but not tetrodotoxin-sensitive sodium channels in DRG neurons.

SCN8A SCN9A

1.08e-05630216029194
Pubmed

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

SCN1A SCN8A

1.51e-05730215272007
Pubmed

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood.

SCN1A SCN8A

1.51e-05730225818041
Pubmed

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

SCN1A SCN8A

2.58e-05930215746173
Pubmed

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

SCN1A SCN8A

2.58e-05930217884088
Pubmed

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

SCN1A SCN8A

4.72e-051230230175250
Pubmed

Genome-wide association study identifies three new melanoma susceptibility loci.

SLC45A2 ATM

6.50e-051430221983787
Pubmed

Blood-Brain Barrier: From Physiology to Disease and Back.

SLC7A3 ATP1A2 SLC16A2

1.02e-0410530330280653
Pubmed

Different evolutionary processes shaped the mouse and human olfactory receptor gene families.

OR8K3 OR5M3 OR2T6 OR5AP2

2.01e-0434030411875048
Pubmed

The olfactory receptor gene superfamily of the mouse.

OR8K3 OR5M3 OR2T6 OR5AP2

2.01e-0434030411802173
Pubmed

A unified nomenclature for vertebrate olfactory receptors.

OR8K3 OR5M3 OR2T6 OR5AP2

2.08e-0434330432295537
Pubmed

Odorant receptor expressed sequence tags demonstrate olfactory expression of over 400 genes, extensive alternate splicing and unequal expression levels.

OR8K3 OR5M3 OR2T6 OR5AP2

2.15e-0434630414611657
Pubmed

E3 ubiquitin ligase RNF123 targets lamin B1 and lamin-binding proteins.

GMPS UBQLNL ATM TNPO2 SCN8A

3.85e-0473630529676528
Pubmed

Identification of new ciliary signaling pathways in the brain and insights into neurological disorders.

ATP1A2 TMEM200A SCN1A SCN9A

3.91e-0440530438187761
InteractionSCN11A interactions

SCN1A SCN8A SCN9A

1.08e-0615283int:SCN11A
InteractionDRD4 interactions

ATM SLC7A3 TNPO2

5.41e-0625283int:DRD4
InteractionSCN5A interactions

SCN1A SCN8A SCN9A

3.74e-0547283int:SCN5A
InteractionSCN4B interactions

SCN1A SCN8A

5.19e-058282int:SCN4B
InteractionLPAR6 interactions

ATM SLC7A3 TNPO2

1.13e-0468283int:LPAR6
InteractionADGRG2 interactions

ATM SLC7A3

1.22e-0412282int:ADGRG2
InteractionNALCN interactions

SCN1A SCN9A

1.68e-0414282int:NALCN
Cytoband11q12.1

OR8K3 OR5M3 OR5AP2

1.60e-0416130311q12.1
CytobandEnsembl 112 genes in cytogenetic band chr11q12

OR8K3 OR5M3 OR5AP2

1.47e-03345303chr11q12
CytobandEnsembl 112 genes in cytogenetic band chr2q24

SCN1A SCN9A

3.14e-03127302chr2q24
CytobandEnsembl 112 genes in cytogenetic band chrXq13

SLC7A3 SLC16A2

5.23e-03165302chrXq13
GeneFamilySodium voltage-gated channel alpha subunits

SCN1A SCN8A SCN9A

1.13e-0792131203
GeneFamilySolute carriers

SLC30A7 SLC45A2 SLC7A3 SLC16A2

1.00e-03395214752
GeneFamilyOlfactory receptors, family 5

OR5M3 OR5AP2

7.40e-03112212152
ToppCellPND07-28-samps-Mesenchymal-Mesenchymal_stem_cell|PND07-28-samps / Age Group, Lineage, Cell class and subclass

UBQLNL SLC7A3 SCN1A

1.06e-04137303ed81624b9167255ce88dcf6ad7f1636376ea0525
ToppCellPND07-28-samps-Mesenchymal-Mesenchymal_stem_cell-Mesenchymal_fibroblast|PND07-28-samps / Age Group, Lineage, Cell class and subclass

UBQLNL SLC7A3 SCN1A

1.06e-0413730347859aa25f32367461c1ec75ed9060bee430c6b7
ToppCellfacs-Marrow-T-cells-24m-Lymphocytic-pre_B_cell|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SEMA6A ATP1A2 SCN9A

1.61e-04158303f296ca24fdedc33f1d24b79e7660763114ce7fa3
ToppCellfacs-Marrow-T-cells-24m-Lymphocytic-precursor_B_cell|Marrow / Spleen_Marrow_Thymus - method, tissue, subtissue, age, lineage, cell ontology and free annotation

SEMA6A ATP1A2 SCN9A

1.61e-041583038c7108f2c40d97a317762ba0b8eca76542b2ebaf
ToppCell390C-Fibroblasts-Fibroblast-B_(Myofibroblast)-|Fibroblasts / Donor, Lineage, Cell class and subclass (all cells)

SEMA6A C1GALT1C1L SCN8A

1.67e-04160303636127753e3a22831f39d4c8170df40901e4329d
ToppCell390C-Fibroblasts-Fibroblast-B_(Myofibroblast)|Fibroblasts / Donor, Lineage, Cell class and subclass (all cells)

SEMA6A C1GALT1C1L SCN8A

1.67e-04160303cb8d0dc1a6c69c7a85c5fdd8f0f6cca1b73dfc63
ToppCellHealthy_donor-CD8+_T_naive|World / disease group, cell group and cell class (v2)

ATM SLC16A2 CYP3A43

1.70e-041613038a61395af33132783a0a37956c6f821aba5d3b1e
ToppCellAdult-Endothelial-endothelial_cell_of_vein-D175|Adult / Lineage, Cell type, age group and donor

HRH1 SEMA6A SLC16A2

1.96e-04169303e1f0298236e4a1c59077c14f0dd29a78fac12648
ToppCellTCGA-Brain|World / Sample_Type by Project: Shred V9

PHKG1 ATP1A2 SCN1A

2.00e-04170303f78e360a6a44d599ec0d207cba4704e50aa314f8
ToppCelllymphoid-B_cell-pro-B|B_cell / Lineage, cell class and subclass

SEMA6A SLC16A2 SCN9A

2.07e-04172303da1e2e54f442f5c2032c857c4812e9060f2053cd
ToppCell5'-Adult-Distal_Rectal-Hematopoietic|Adult / Celltypes from developing, pediatric, Crohn's, & adult GI tract

RIC8B SCN8A SCN9A

2.10e-04173303b335ca2a247156eba821943b2b9fc9922230b409
ToppCellwk_15-18-Mesenchymal-Chondrocyte-intermediate_chondrocyte|wk_15-18 / Celltypes from embryonic and fetal-stage human lung

SEMA6A ATP1A2 SCN1A

2.17e-04175303a84965d28438a4228d841b357c2cd75cf4b59a63
ToppCell3'-GW_trimst-1.5-LargeIntestine-Neuronal-Glial_immature-Glia_3_(BCAN+)|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ATP1A2 SCN1A SCN9A

2.25e-04177303d05497d2c80a66ec6a4e1733fea3a5534877a6a7
ToppCell3'-GW_trimst-1.5-LargeIntestine-Neuronal-Glial_immature|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ATP1A2 SCN1A SCN9A

2.44e-04182303ecb5624c9074cc6449fad961df54c926c2681d54
ToppCellLPS-IL1RA|World / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

SLC30A7 HRH1 SEMA6A

2.52e-04184303c066c2ec4f0f1d6eb183fca5c7bb0cd45c9950dc
ToppCellCOVID_vent-Myeloid-Dendritic|COVID_vent / Disease condition, Lineage, Cell class and subclass

SLC45A2 SLC7A3 SCN9A

2.60e-0418630363a5cdd3f60681762a218be32db84be8f29b88fd
ToppCellCOVID_vent-Myeloid-Dendritic-cDC|COVID_vent / Disease condition, Lineage, Cell class and subclass

SLC45A2 SLC7A3 SCN9A

2.60e-0418630339457a7b43537f2c3e221f9375c95d4515424d7d
ToppCellControl-Endothelial-Endothelial-Alv_Cap|Control / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.64e-04187303ea9d34bcd3bd1f36745846309ede349773de501a
ToppCellLPS-IL1RA+antiTNF-Endothelial-Endothelial-Activated_Alv_Cap|LPS-IL1RA+antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.64e-04187303f3397dbc23b6c2f24e2c1ba887d8f9aef3ee01a1
ToppCellLPS-IL1RA+antiTNF-Endothelial-Endothelial-Alv_Cap|LPS-IL1RA+antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.68e-0418830373f6ec915934154f435a376cb274b058ff7c5f35
ToppCellControl-Endothelial-Endothelial-Alv_Gen_Intermediate|Control / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.72e-041893035d7ae1ead7f4fbaeec26f651833c9c2106e1e4d1
ToppCellLPS_only-Endothelial-Endothelial-Alv_Cap|LPS_only / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.77e-04190303474cbbab8f3b0a6881fa6c92edb78e43999f9ab0
ToppCellLPS-IL1RA+antiTNF-Endothelial-Endothelial-Alv_Gen_Intermediate|LPS-IL1RA+antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.77e-04190303a3c6eec6df052105ab78b7e3c78f94218d5912eb
ToppCellLPS-IL1RA-Endothelial-Endothelial-Alv_Gen_Intermediate|LPS-IL1RA / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.77e-04190303106ea0bb7b99c697ffc5443d72343df2484250c7
ToppCellLPS_only-Endothelial-Endothelial-Activated_Alv_Cap|LPS_only / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.81e-04191303a7b18bcf27c38ad2353c239ecb309c80f3ef3359
ToppCellPCW_05-06-Mesenchymal-Mesenchymal_fibroblastic-mes_chondroblast_(18)|PCW_05-06 / Celltypes from embryonic and fetal-stage human lung

SEMA6A ATP1A2 SCN1A

2.85e-04192303d0649410cf5eacdb0c1dce70e37c7473ef5fddfa
ToppCellLPS-antiTNF-Endothelial-Endothelial-Activated_Alv_Cap|LPS-antiTNF / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.85e-04192303c618ede75dce3988c87a5b8f98d8e94e1dd66efd
ToppCellControl-Endothelial-Endothelial|Control / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.90e-04193303aff0649c73c634bc6ff0dc7759b4693a9236bf05
ToppCellControl-Endothelial|Control / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.90e-04193303c5f9fe03e64c211d4bcd4959e5b32f14841e336a
ToppCellLPS-IL1RA-Endothelial-Endothelial-Activated_Alv_Cap|LPS-IL1RA / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.90e-04193303a3636c35ed25aabe2f1aba016c9fe125327bbfaf
ToppCell5'-GW_trimst-1.5-LargeIntestine-Neuronal-Glial_immature|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ATP1A2 SCN1A SCN9A

2.90e-04193303cdc44bf6f5436eb8a2d4720fe011dcb85ccecf87
ToppCell3'-GW_trimst-1.5-LargeIntestine-Neuronal|GW_trimst-1.5 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ATP1A2 SCN1A SCN9A

2.90e-0419330366af80f4b51e1ce97b6fb7c630dc5f95bfa7e7d4
ToppCellLPS-IL1RA-Endothelial-Endothelial|LPS-IL1RA / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.94e-041943031d39d968730a7e85b6161c1c8a6bd38afe9bcad7
ToppCellLPS-IL1RA-Endothelial|LPS-IL1RA / V2 postpublication: Rhesus Genome Updated; Treatment groups by lineage, cell_type_level1, cell_type_level2

HRH1 SEMA6A SCN9A

2.94e-0419430343f92b0533e26633dc94cce554045d641ef8fd76
ToppCellTracheal-10x5prime-Stromal-Chondrocytic|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations

UBQLNL ATP1A2 CYP3A43

3.12e-04198303c72ef2ddcbb6dacbed4c6200d89e17d57314dcdc
ToppCellTracheal-10x5prime-Stromal-Chondrocytic-Chondrocyte|10x5prime / Cell types per location group and 10X technology with lineage, and cell group designations

UBQLNL ATP1A2 CYP3A43

3.12e-0419830355f013e9e6587d9ece59751fa131b1d22d6cceea
ToppCell3'-GW_trimst-1-LargeIntestine-Neuronal-Glial_immature-ENCC/glia_Progenitor|GW_trimst-1 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

ATP1A2 SCN1A SCN9A

3.17e-041993038d13a9ea87f685b5a34b84c4571db6be753cf2d9
Drugthephorin

HRH1 SEMA6A

1.68e-062302CID000011290
Drugethacizine

HRH1 SCN9A

1.01e-054302CID000107841
Diseasegeneralized epilepsy with febrile seizures plus 2 (implicated_via_orthology)

SCN1A SCN8A SCN9A

9.14e-0810283DOID:0111294 (implicated_via_orthology)
DiseaseDravet syndrome (implicated_via_orthology)

SCN1A SCN8A SCN9A

9.14e-0810283DOID:0080422 (implicated_via_orthology)
Diseasegeneralized epilepsy with febrile seizures plus (implicated_via_orthology)

SCN1A SCN8A SCN9A

1.67e-0712283DOID:0060170 (implicated_via_orthology)
DiseaseEarly Infantile Epileptic Encephalopathy 6

SCN1A SCN9A

8.68e-072282C4551549
DiseaseB Virus Infection

SCN8A SCN9A

2.60e-063282C0037140
DiseaseFamilial or sporadic hemiplegic migraine

ATP1A2 SCN1A

2.60e-063282cv:CN295307
DiseasePostherpetic neuralgia

SCN8A SCN9A

2.60e-063282C0032768
DiseaseHerpesviridae Infections

SCN8A SCN9A

2.60e-063282C0019372
DiseaseFamilial hemiplegic migraine

ATP1A2 SCN1A

2.60e-063282cv:C0338484
DiseaseCerebral Small Vessel Diseases

ATP1A2 SCN1A

8.67e-065282C2733158
DiseaseFamilial benign neonatal epilepsy

ATP1A2 SCN8A

1.30e-056282C0220669
Diseaseepilepsy (implicated_via_orthology)

ATP1A2 SCN1A SCN8A SCN9A

1.66e-05163284DOID:1826 (implicated_via_orthology)
DiseaseEarly Childhood Epilepsy, Myoclonic

SCN1A SCN9A

2.42e-058282C0393695
DiseaseIdiopathic Myoclonic Epilepsy

SCN1A SCN9A

2.42e-058282C0338478
DiseaseSymptomatic Myoclonic Epilepsy

SCN1A SCN9A

2.42e-058282C0338479
DiseaseMyoclonic Encephalopathy

SCN1A SCN9A

2.42e-058282C0438414
DiseaseBenign Infantile Myoclonic Epilepsy

SCN1A SCN9A

2.42e-058282C0751120
DiseaseMyoclonic Absence Epilepsy

SCN1A SCN9A

2.42e-058282C0393703
DiseasePruritus

HRH1 SCN9A

2.42e-058282C0033774
DiseaseMyoclonic Epilepsy

SCN1A SCN9A

3.11e-059282C0014550
DiseaseGeneralized Epilepsy with Febrile Seizures Plus

SCN1A SCN9A

3.11e-059282C3502809
DiseaseEpilepsy, Myoclonic, Infantile

SCN1A SCN9A

3.89e-0510282C0917800
DiseaseMyoclonic Astatic Epilepsy

SCN1A SCN9A

4.75e-0511282C0393702
DiseaseInfantile Severe Myoclonic Epilepsy

SCN1A SCN9A

6.73e-0513282C0751122
DiseaseEpilepsy

SCN1A SCN8A SCN9A

1.50e-04109283C0014544
Diseaseanxiety disorder (implicated_via_orthology)

SCN1A SCN9A

1.98e-0422282DOID:2030 (implicated_via_orthology)
DiseaseMental Retardation, Psychosocial

SCN1A CAPN10 SCN8A

3.07e-04139283C0025363
DiseaseProfound Mental Retardation

SCN1A CAPN10 SCN8A

3.07e-04139283C0020796
DiseaseMental deficiency

SCN1A CAPN10 SCN8A

3.07e-04139283C0917816
DiseaseInherited neuropathies

ATM SCN9A

6.62e-0440282C0598589

Protein segments in the cluster

PeptideGeneStartEntry
YMLLVGNIIMMPDAQ

ERVK13-1

211

Q9NX77
MMGDSMVKINGIYLT

ARMC2

166

Q8NEN0
MLGQFLQEVSIMAVM

CAPN10

656

Q9HC96
PMQASQAIGYLLGMM

SLC16A2

441

P36021
FMAMIANGVMIFLIN

OR2T6

36

Q8NHC8
VVYIITMVGNIGMMV

OR5M3

31

Q8NGP4
YMANMVGNLGMIVLI

OR5AP2

41

Q8NGF4
YQLAARMGTKMMGGL

ATM

2521

Q13315
LISMAYGQIGMIQAL

ATP1A2

846

P50993
LGICYGMQMMNKVFG

GMPS

101

P49915
YGVQAGMKMIEQMLK

BPIFC

41

Q8NFQ6
MWGLYEGQQPMLVIM

CYP3A43

71

Q9HB55
NGLTPQKMEVMMYGL

C1GALT1C1L

276

P0DN25
VGAVVMPMNILYLLM

HRH1

76

P35367
ILTLGVMMLVGMALY

SLC45A2

106

Q9UMX9
VMMLVGMALYLNGAT

SLC45A2

111

Q9UMX9
SIFVNIYLMMQMTAG

SLC7A3

551

Q8WY07
MLMLRMIMSGNYQFG

PHKG1

236

Q16816
KEQRQMNGMYTGLMG

TMEM200A

176

Q86VY9
TMVYNGMNMEAIHVL

RIC8B

331

Q9NVN3
IVYMMVMVIGNLVVL

SCN9A

946

Q15858
MVLMQMGQPALLYLV

SPPL2C

491

Q8IUH8
FLMIYVISVMGNLGM

OR8K3

31

Q8NH51
VFMMVMVIGNLVVLN

SCN1A

971

P35498
YIKVVMQNGRMMGAV

PYROXD1

446

Q8WU10
LDIQMIMIMNGTLYI

SEMA6A

56

Q9H2E6
MGAEMQPYVQMVLNN

TNPO2

736

O14787
VFMMVMVIGNLVVLN

SCN8A

956

Q9UQD0
TGGMMQLLMNNPYLA

UBQLNL

426

Q8IYU4
VIASAIMMQNFGLMI

SLC30A7

251

Q8NEW0
VLNMLMMTAVNGVAV

ZNF862

1061

O60290
GVMYLKLVLGQMVQA

nan

66

Q6AWC8