Cluster composition

Functions

CategoryNameIntersectionWithQueryPValueGenesInTermGenesInQueryGenesInTermInQueryID
GeneOntologyMolecularFunctionolfactory receptor activity

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

3.66e-104318515GO:0004984
GeneOntologyMolecularFunctionG protein-coupled receptor activity

OR2F2 OR8U1 ADRB3 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

4.18e-098848519GO:0004930
GeneOntologyMolecularFunctiontransmembrane signaling receptor activity

GABRG2 OR2F2 OR8U1 ADRB3 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 OR10R2 CHRNA3 OR8U9 OR8U8 OR1L4 OR52J3

1.59e-0713538521GO:0004888
GeneOntologyMolecularFunctionsodium ion transmembrane transporter activity

SLC9A2 SLC38A4 SCN1A SCN2A SLC9C2 CNGB1

9.03e-05171856GO:0015081
GeneOntologyMolecularFunctionmonoatomic ion transmembrane transporter activity

GABRG2 SLC9A2 TMC7 SLC15A1 SLC38A4 SCN1A SCN2A CFTR SLC36A3 SLC9C2 CNGB1 CHRNA3

1.30e-047938512GO:0015075
GeneOntologyMolecularFunctionodorant binding

OR8U1 OR14A2 OR10R2 OR8U9 OR8U8

2.10e-04127855GO:0005549
GeneOntologyMolecularFunctiontransmembrane transporter activity

GABRG2 SLC9A2 TMC7 ABCB9 SLC15A1 SLC38A4 SCN1A SCN2A CFTR SLC36A3 SLC9C2 CNGB1 ABCA10 CHRNA3

4.33e-0411808514GO:0022857
GeneOntologyMolecularFunctiongated channel activity

GABRG2 TMC7 SCN1A SCN2A CFTR CNGB1 CHRNA3

5.56e-04334857GO:0022836
GeneOntologyMolecularFunctionpeptide transmembrane transporter activity

ABCB9 SLC15A1

6.32e-049852GO:1904680
GeneOntologyMolecularFunctionG protein-coupled amine receptor activity

ADRB3 HRH4 TAAR8

7.06e-0441853GO:0008227
GeneOntologyMolecularFunctionepoxide hydrolase activity

EPHX1 ALOX12

9.61e-0411852GO:0004301
GeneOntologyMolecularFunctionactive transmembrane transporter activity

SLC9A2 ABCB9 SLC15A1 SLC38A4 CFTR SLC36A3 SLC9C2 ABCA10

9.63e-04477858GO:0022804
GeneOntologyMolecularFunctiontransporter activity

GABRG2 SLC9A2 TMC7 ABCB9 SLC15A1 SLC38A4 SCN1A SCN2A CFTR SLC36A3 SLC9C2 CNGB1 ABCA10 CHRNA3

1.03e-0312898514GO:0005215
GeneOntologyMolecularFunctionABC-type transporter activity

ABCB9 CFTR ABCA10

1.19e-0349853GO:0140359
GeneOntologyMolecularFunctionhydrolase activity, acting on ether bonds

EPHX1 ALOX12

1.35e-0313852GO:0016801
GeneOntologyMolecularFunctionether hydrolase activity

EPHX1 ALOX12

1.35e-0313852GO:0016803
GeneOntologyMolecularFunctioninorganic molecular entity transmembrane transporter activity

GABRG2 SLC9A2 SLC15A1 SLC38A4 SCN1A SCN2A CFTR SLC36A3 SLC9C2 CNGB1

1.40e-037588510GO:0015318
GeneOntologyMolecularFunctionsodium channel activity

SCN1A SCN2A CNGB1

1.42e-0352853GO:0005272
GeneOntologyMolecularFunctionpotassium:proton antiporter activity

SLC9A2 SLC9C2

1.58e-0314852GO:0015386
GeneOntologyMolecularFunctionsodium ion binding

SCN1A SCN2A

1.58e-0314852GO:0031402
GeneOntologyMolecularFunctionmonoatomic cation transmembrane transporter activity

SLC9A2 SLC15A1 SLC38A4 SCN1A SCN2A SLC36A3 SLC9C2 CNGB1 CHRNA3

2.04e-03664859GO:0008324
GeneOntologyMolecularFunctionsodium:proton antiporter activity

SLC9A2 SLC9C2

2.07e-0316852GO:0015385
GeneOntologyMolecularFunctionalanine transmembrane transporter activity

SLC38A4 SLC36A3

2.07e-0316852GO:0022858
GeneOntologyMolecularFunctionoligopeptide transmembrane transporter activity

ABCB9 SLC15A1

2.07e-0316852GO:0035673
GeneOntologyMolecularFunctionvoltage-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential

SCN1A SCN2A

2.34e-0317852GO:0099508
GeneOntologyMolecularFunctionsolute:potassium antiporter activity

SLC9A2 SLC9C2

2.92e-0319852GO:0022821
GeneOntologyMolecularFunctionmonoatomic ion channel activity

GABRG2 TMC7 SCN1A SCN2A CFTR CNGB1 CHRNA3

3.42e-03459857GO:0005216
GeneOntologyMolecularFunctionpostsynaptic neurotransmitter receptor activity

GABRG2 HRH4 CHRNA3

4.03e-0375853GO:0098960
GeneOntologyMolecularFunctionacetylcholine receptor activity

HRH4 CHRNA3

4.28e-0323852GO:0015464
GeneOntologyBiologicalProcessdetection of chemical stimulus involved in sensory perception of smell

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

1.81e-114328416GO:0050911
GeneOntologyBiologicalProcesssensory perception of smell

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

5.39e-114658416GO:0007608
GeneOntologyBiologicalProcessdetection of chemical stimulus involved in sensory perception

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

1.00e-104858416GO:0050907
GeneOntologyBiologicalProcessdetection of stimulus involved in sensory perception

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 SCN1A OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

1.60e-105828417GO:0050906
GeneOntologyBiologicalProcessdetection of chemical stimulus

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

3.12e-105248416GO:0009593
GeneOntologyBiologicalProcesssensory perception of chemical stimulus

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

5.82e-105478416GO:0007606
GeneOntologyBiologicalProcessdetection of stimulus

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 SCN1A OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

4.21e-097228417GO:0051606
GeneOntologyBiologicalProcessG protein-coupled receptor signaling pathway

OR2F2 OR8U1 ADRB3 OR14A2 GNA14 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 CNGB1 OR10R2 ADCY6 OR8U9 OR8U8 OR1L4 OR52J3

2.51e-0813958422GO:0007186
GeneOntologyBiologicalProcesssensory perception

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 SCN1A OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

1.22e-0610728417GO:0007600
GeneOntologyBiologicalProcessmembrane depolarization

SCN1A SCN2A CFTR CNGB1 ALOX12 CHRNA3

1.01e-05121846GO:0051899
GeneOntologyBiologicalProcesssodium ion transmembrane transport

SLC9A2 SLC38A4 SCN1A SCN2A CFTR SLC9C2 CNGB1

2.25e-05208847GO:0035725
GeneOntologyBiologicalProcesssodium ion transport

SLC9A2 SLC38A4 SCN1A SCN2A CFTR SLC9C2 CNGB1

1.31e-04275847GO:0006814
GeneOntologyBiologicalProcessepoxide metabolic process

EPHX1 ALOX12

1.63e-045842GO:0097176
GeneOntologyBiologicalProcessdiencephalon morphogenesis

OTX1 OTX2

2.43e-046842GO:0048852
GeneOntologyBiologicalProcessregulation of membrane potential

GABRG2 GNA14 SCN1A SCN2A CFTR CNGB1 ALOX12 CHRNA3 CNTF

4.48e-04559849GO:0042391
GeneOntologyBiologicalProcessglutamate catabolic process

GAD2 GLUD1

4.52e-048842GO:0006538
HumanPhenoPhotosensitive myoclonic seizure

GABRG2 SCN1A SCN2A

2.86e-068203HP:0001327
HumanPhenoCyanotic episode

GABRG2 SCN1A SCN2A

2.86e-068203HP:0200048
HumanPhenoLimited neck range of motion

GABRG2 SCN1A SCN2A

8.37e-0611203HP:0000466
HumanPhenoEpilepsia partialis continua

GABRG2 SCN1A SCN2A

1.11e-0512203HP:0012847
HumanPhenoGeneralized cerebral atrophy/hypoplasia

GABRG2 SCN1A SCN2A

1.44e-0513203HP:0007058
HumanPhenoFacial tics

GABRG2 SCN1A SCN2A

2.29e-0515203HP:0011468
HumanPhenoPhotosensitive tonic-clonic seizure

GABRG2 SCN1A SCN2A

2.29e-0515203HP:0007207
HumanPhenoDysgenesis of the hippocampus

GABRG2 SCN1A SCN2A

2.81e-0516203HP:0025101
HumanPhenoComplex febrile seizure

GABRG2 SCN1A SCN2A

2.81e-0516203HP:0011172
HumanPhenoFocal motor status epilepticus

GABRG2 SCN1A SCN2A

3.40e-0517203HP:0032663
HumanPhenoAtypical absence status epilepticus

GABRG2 SCN1A SCN2A

3.40e-0517203HP:0011151
HumanPhenoVisually-induced seizure

GABRG2 SCN1A SCN2A

4.07e-0518203HP:0020216
HumanPhenoGeneralized non-convulsive status epilepticus without coma

GABRG2 SCN1A SCN2A

4.07e-0518203HP:0032860
HumanPhenoNon-convulsive status epilepticus without coma

GABRG2 SCN1A SCN2A

5.66e-0520203HP:0032671
HumanPhenoTalipes valgus

GABRG2 SCN1A SCN2A

6.58e-0521203HP:0004684
HumanPhenoReflex seizure

GABRG2 SCN1A SCN2A

7.60e-0522203HP:0020207
HumanPhenoTibial torsion

GABRG2 SCN1A SCN2A

8.72e-0523203HP:0100694
HumanPhenoEEG with spike-wave complexes (>3.5 Hz)

GABRG2 SCN1A

8.75e-054202HP:0010849
HumanPhenoMultifocal epileptiform discharges

GABRG2 SCN1A SCN2A ARFGEF1

1.07e-0466204HP:0010841
HumanPhenoFocal hemiclonic seizure

GABRG2 SCN1A SCN2A

1.13e-0425203HP:0006813
HumanPhenoLimited knee extension

GABRG2 SCN1A SCN2A

1.43e-0427203HP:0003066
HumanPhenoStatus epilepticus without prominent motor symptoms

GABRG2 SCN1A SCN2A

1.43e-0427203HP:0031475
HumanPhenoFocal aware seizure

GABRG2 SCN1A SCN2A

1.59e-0428203HP:0002349
HumanPhenoStatus epilepticus with prominent motor symptoms

GABRG2 SCN1A SCN2A

1.77e-0429203HP:0032658
HumanPhenoProgressive gait ataxia

GABRG2 SCN1A SCN2A

1.96e-0430203HP:0007240
HumanPhenoProgressive ataxia

GABRG2 SCN1A SCN2A

1.96e-0430203HP:0001329
HumanPhenoCogwheel rigidity

GABRG2 SCN1A SCN2A

2.39e-0432203HP:0002396
HumanPhenoObsessive-compulsive trait

GABRG2 SCN1A SCN2A

2.62e-0433203HP:0008770
HumanPhenoGeneralized clonic seizure

GABRG2 SCN1A SCN2A

2.87e-0434203HP:0011169
HumanPhenoCalcaneovalgus deformity

GABRG2 SCN1A SCN2A

2.87e-0434203HP:0001848
HumanPhenoDeformed tarsal bones

GABRG2 SCN1A SCN2A

3.13e-0435203HP:0008119
HumanPhenoLimitation of knee mobility

GABRG2 SCN1A SCN2A

3.13e-0435203HP:0010501
HumanPhenoLimitation of neck motion

GABRG2 SCN1A SCN2A

3.40e-0436203HP:0005986
HumanPhenoAbnormal neck physiology

GABRG2 SCN1A SCN2A

3.40e-0436203HP:0025669
HumanPhenoDisturbance of facial expression

GABRG2 SCN1A SCN2A

3.40e-0436203HP:0005324
HumanPhenoAtonic seizure

GABRG2 SCN1A SCN2A ARFGEF1

4.20e-0494204HP:0010819
HumanPhenoAbnormal ankle morphology

GABRG2 SCN1A SCN2A STAT4

5.32e-04100204HP:0034673
HumanPhenoFocal clonic seizure

GABRG2 SCN1A SCN2A

5.39e-0442203HP:0002266
HumanPhenoLate young adult onset

GDAP2 ANXA11 TMEM126B

5.78e-0443203HP:0025710
HumanPhenoAtypical absence seizure

GABRG2 SCN1A SCN2A

7.06e-0446203HP:0007270
HumanPhenoAbnormal hippocampus morphology

GABRG2 SCN1A SCN2A

8.00e-0448203HP:0025100
HumanPhenoAbnormal morphology of the limbic system

GABRG2 SCN1A SCN2A

8.50e-0449203HP:0007343
HumanPhenoHypermetric saccades

GDAP2 VPS41

9.44e-0412202HP:0007338
HumanPhenoFocal automatism seizure

SCN1A SCN2A

9.44e-0412202HP:0032898
HumanPhenoEEG with focal epileptiform discharges

GABRG2 SCN1A SCN2A ARFGEF1

9.95e-04118204HP:0011185
HumanPhenoBilateral tonic-clonic seizure with focal onset

GABRG2 SCN1A SCN2A

1.01e-0352203HP:0007334
HumanPhenoBilateral tonic-clonic seizure with generalized onset

GABRG2 SCN1A SCN2A

1.01e-0352203HP:0025190
HumanPhenoEEG with irregular generalized spike and wave complexes

GABRG2 SCN1A

1.11e-0313202HP:0001326
HumanPhenoAbnormality of salivation

GABRG2 SCN1A SCN2A ANXA11 STAT4

1.18e-03215205HP:0100755
HumanPhenoCortical dysplasia

GABRG2 SCN1A SCN2A

1.26e-0356203HP:0002539
HumanPhenoPes valgus

GABRG2 SCN1A SCN2A

1.26e-0356203HP:0008081
HumanPhenoMyoclonic absence seizure

GABRG2 SCN1A

1.30e-0314202HP:0011150
HumanPhenoAbnormality of the calcaneus

GABRG2 SCN1A SCN2A

1.32e-0357203HP:0008364
HumanPhenoAortopulmonary collateral arteries

SCN1A SCN2A

1.49e-0315202HP:0031834
DomainGPCR_Rhodpsn_7TM

OR2F2 OR8U1 ADRB3 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

6.52e-106708318IPR017452
Domain7tm_1

OR2F2 OR8U1 ADRB3 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

7.69e-106778318PF00001
DomainG_PROTEIN_RECEP_F1_1

OR2F2 OR8U1 ADRB3 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

9.27e-106858318PS00237
DomainG_PROTEIN_RECEP_F1_2

OR2F2 OR8U1 ADRB3 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

1.07e-096918318PS50262
DomainGPCR_Rhodpsn

OR2F2 OR8U1 ADRB3 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 CCRL2 HRH4 TAAR8 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

1.09e-096928318IPR000276
DomainOlfact_rcpt

OR2F2 OR8U1 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

1.88e-093938314IPR000725
DomainOtx_TF

OTX1 OTX2

1.95e-052832IPR003025
DomainArp3_met

ACTR3B ACTR3

5.84e-053832IPR015623
DomainOtx_TF_C

OTX1 OTX2

5.84e-053832IPR013851
DomainTF_Otx

OTX1 OTX2

5.84e-053832PF03529
DomainNa_trans_cytopl

SCN1A SCN2A

2.89e-046832PF11933
DomainNa_trans_cytopl

SCN1A SCN2A

2.89e-046832IPR024583
DomainABC_transporter_CS

ABCB9 CFTR ABCA10

8.57e-0442833IPR017871
DomainNa_channel_asu

SCN1A SCN2A

8.58e-0410832IPR001696
DomainNa_trans_assoc

SCN1A SCN2A

8.58e-0410832IPR010526
DomainNa_trans_assoc

SCN1A SCN2A

8.58e-0410832PF06512
DomainCation/H_exchanger_CPA1

SLC9A2 SLC9C2

1.05e-0311832IPR018422
DomainABC_tran

ABCB9 CFTR ABCA10

1.27e-0348833PF00005
DomainABC_TRANSPORTER_2

ABCB9 CFTR ABCA10

1.27e-0348833PS50893
DomainABC_TRANSPORTER_1

ABCB9 CFTR ABCA10

1.35e-0349833PS00211
DomainABC_transporter-like

ABCB9 CFTR ABCA10

1.43e-0350833IPR003439
DomainNa_H_Exchanger

SLC9A2 SLC9C2

1.72e-0314832PF00999
DomainCation/H_exchanger

SLC9A2 SLC9C2

1.72e-0314832IPR006153
DomainChannel_four-helix_dom

SCN1A SCN2A SLC9C2

2.08e-0357833IPR027359
Domain-

SCN1A SCN2A SLC9C2

2.08e-03578331.20.120.350
DomainAa_trans

SLC38A4 SLC36A3

2.54e-0317832PF01490
DomainAA_transpt_TM

SLC38A4 SLC36A3

2.54e-0317832IPR013057
DomainActin/actin-like_CS

ACTR3B ACTR3

2.85e-0318832IPR020902
Domain-

CIP2A EFR3B ARFGEF1 PSMD5 CHIC1

3.11e-032228351.25.10.10
DomainACTINS_ACT_LIKE

ACTR3B ACTR3

3.18e-0319832PS01132
DomainAAA+_ATPase

ABCB9 CFTR SNRNP200 ABCA10

3.89e-03144834IPR003593
DomainAAA

ABCB9 CFTR SNRNP200 ABCA10

3.89e-03144834SM00382
DomainABC_membrane

ABCB9 CFTR

5.05e-0324832PF00664
DomainABC_TM1F

ABCB9 CFTR

6.84e-0328832PS50929
DomainABC1_TM_dom

ABCB9 CFTR

6.84e-0328832IPR011527
DomainARM-like

CIP2A EFR3B ARFGEF1 PSMD5 CHIC1

7.07e-03270835IPR011989
DomainActin

ACTR3B ACTR3

8.35e-0331832IPR004000
DomainActin

ACTR3B ACTR3

8.35e-0331832PF00022
DomainACTIN

ACTR3B ACTR3

8.35e-0331832SM00268
DomainCNMP_BINDING_1

SLC9C2 CNGB1

8.88e-0332832PS00888
DomainCNMP_BINDING_2

SLC9C2 CNGB1

8.88e-0332832PS00889
PathwayREACTOME_OLFACTORY_SIGNALING_PATHWAY

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

5.70e-114176616M4072
PathwayKEGG_OLFACTORY_TRANSDUCTION

OR2F2 OR8U1 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 OR13C2 OR2F1 CNGB1 OR10R2 OR8U8 OR1L4 OR52J3

2.47e-093896614M14091
PathwayREACTOME_SENSORY_PERCEPTION

OR2F2 OR8U1 OR14A2 OR13C9 OR13C5 OR51B6 OR13C3 OR13C4 SCN2A OR13C2 OR2F1 CNGB1 OR10R2 OR8U9 OR8U8 OR1L4 OR52J3

3.42e-096366617M41834
Pubmed

Organization and evolutionary relatedness of OR37 olfactory receptor genes in mouse and human.

OR13C9 OR13C5 OR13C3 OR13C4 OR13C2

6.42e-111286512906860
Pubmed

The human olfactory receptor gene family.

OR2F2 OR13C9 OR13C5 OR13C3 OR13C4 OR13C2 OR2F1 OR10R2 OR1L4 OR52J3

9.38e-07541861014983052
Pubmed

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

EPHX1 SCN1A SCN2A

1.73e-061086320602612
Pubmed

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

OR2F2 OR8U1 OR14A2 OR51B6 OR13C3 OR2F1 OR1L4 OR52J3

2.10e-0634086811875048
Pubmed

The olfactory receptor gene superfamily of the mouse.

OR2F2 OR8U1 OR14A2 OR51B6 OR13C3 OR2F1 OR1L4 OR52J3

2.10e-0634086811802173
Pubmed

A unified nomenclature for vertebrate olfactory receptors.

OR2F2 OR8U1 OR14A2 OR51B6 OR13C3 OR2F1 OR1L4 OR52J3

2.24e-0634386832295537
Pubmed

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

OR2F2 OR8U1 OR14A2 OR51B6 OR13C3 OR2F1 OR1L4 OR52J3

2.39e-0634686814611657
Pubmed

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

SCN1A SCN2A

6.04e-06286229649454
Pubmed

Otx genes and the genetic control of brain morphogenesis.

OTX1 OTX2

6.04e-06286210049527
Pubmed

Otx2 controls identity and fate of glutamatergic progenitors of the thalamus by repressing GABAergic differentiation.

OTX1 OTX2

6.04e-06286216738237
Pubmed

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.

GABRG2 SCN1A

6.04e-06286218566737
Pubmed

Differential transcriptional control as the major molecular event in generating Otx1-/- and Otx2-/- divergent phenotypes.

OTX1 OTX2

6.04e-06286210068635
Pubmed

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

SCN1A SCN2A

6.04e-06286210827969
Pubmed

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

SCN1A SCN2A

6.04e-06286219694741
Pubmed

Function and evolution of Otx proteins.

OTX1 OTX2

6.04e-06286210375352
Pubmed

Does a SCN1A gene mutation confer earlier age of onset of febrile seizures in GEFS+?

GABRG2 SCN1A

6.04e-06286219292758
Pubmed

ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cells.

ACTR3B ACTR3

6.04e-06286210806390
Pubmed

Differential expression of two sodium channel subtypes in human brain.

SCN1A SCN2A

6.04e-0628621317301
Pubmed

From fly head to mammalian forebrain: the story of otd and Otx.

OTX1 OTX2

6.04e-0628627974744
Pubmed

Otx1 and Otx2 in the development and evolution of the mammalian brain.

OTX1 OTX2

6.04e-0628629843484
Pubmed

Gene and domain duplication in the chordate Otx gene family: insights from amphioxus Otx.

OTX1 OTX2

6.04e-0628629580990
Pubmed

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

SCN1A SCN2A

6.04e-06286233096315
Pubmed

Otx1 and Otx2 define layers and regions in developing cerebral cortex and cerebellum.

OTX1 OTX2

6.04e-0628627931541
Pubmed

Differentiation of cerebellar cell identities in absence of Fgf signalling in zebrafish Otx morphants.

OTX1 OTX2

6.04e-06286216611693
Pubmed

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

SCN1A SCN2A

6.04e-06286231439038
Pubmed

Structural evolution of Otx genes in craniates.

OTX1 OTX2

6.04e-06286211504847
Pubmed

OTX2 regulates CFTR expression during endoderm differentiation and occupies 3' cis-regulatory elements.

OTX2 CFTR

6.04e-06286233386644
Pubmed

Association analysis of gamma2 subunit of gamma-aminobutyric acid (GABA) type A receptor and voltage-gated sodium channel type II alpha-polypeptide gene mutation in southern Chinese children with febrile seizures.

GABRG2 SCN2A

6.04e-06286217641256
Pubmed

Otx genes in corticogenesis and brain development.

OTX1 OTX2

6.04e-06286210498271
Pubmed

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

SCN1A SCN2A

6.04e-06286226311622
Pubmed

Expression of the homeobox genes OTX2 and OTX1 in the early developing human brain.

OTX1 OTX2

6.04e-06286220354145
Pubmed

Evolution and homology of the nervous system: cross-phylum rescues of otd/Otx genes.

OTX1 OTX2

6.04e-0628629635399
Pubmed

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

SCN1A SCN2A

6.04e-06286215249644
Pubmed

Genomic regulation of natural variation in cortical and noncortical brain volume.

OTX1 CNTF

6.04e-06286216503985
Pubmed

Otx2 expression in anterior neuroectoderm and forebrain/midbrain is directed by more than six enhancers.

OTX1 OTX2

6.04e-06286224457099
Pubmed

Polymorphic Variants of SCN1A and EPHX1 Influence Plasma Carbamazepine Concentration, Metabolism and Pharmacoresistance in a Population of Kosovar Albanian Epileptic Patients.

EPHX1 SCN1A

6.04e-06286226555147
Pubmed

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

SCN1A SCN2A

6.04e-06286221377452
Pubmed

Genetic screening of two Tunisian families with generalized epilepsy with febrile seizures plus.

GABRG2 SCN1A

6.04e-06286219236456
Pubmed

Developmental rescue of Drosophila cephalic defects by the human Otx genes.

OTX1 OTX2

6.04e-0628629520436
Pubmed

OTX1 and OTX2 as possible molecular markers of sinonasal carcinomas and olfactory neuroblastomas.

OTX1 OTX2

6.04e-06286228348423
Pubmed

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

SCN1A SCN2A

6.04e-06286230693367
Pubmed

Genetic and molecular roles of Otx homeodomain proteins in head development.

OTX1 OTX2

6.04e-06286210767524
Pubmed

OTX1 and OTX2 Genes in Medulloblastoma.

OTX1 OTX2

6.04e-06286230797919
Pubmed

Kv7/KCNQ potassium channels in cortical hyperexcitability and juvenile seizure-related death in Ank2-mutant mice.

GABRG2 GAD2 SCN2A

1.16e-051886337321992
Pubmed

Chromosomal localization of the mouse genes coding for alpha 2, alpha 3, alpha 4 and beta 2 subunits of neuronal nicotinic acetylcholine receptor.

GLUD1 ME1 CHRNA3

1.16e-05188632338144
Pubmed

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

SCN1A SCN2A

1.81e-05386228784306
Pubmed

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

SCN1A SCN2A

1.81e-05386232185219
Pubmed

Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies.

GABRG2 SCN1A

1.81e-05386219522081
Pubmed

Sodium channels SCN1A, SCN2A and SCN3A in familial autism.

SCN1A SCN2A

1.81e-05386212610651
Pubmed

Otx5 regulates genes that show circadian expression in the zebrafish pineal complex.

OTX1 OTX2

1.81e-05386211753388
Pubmed

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

SCN1A SCN2A

1.81e-05386232005694
Pubmed

GEFS+ is not related to the most common mutations of SCN1B, SCN1A and GABRG2 in two Tunisian families.

GABRG2 SCN1A

1.81e-05386218175077
Pubmed

Generalised epilepsy with febrile seizures plus (GEFS(+)): molecular analysis in a restricted area.

GABRG2 SCN1A

1.81e-05386222011963
Pubmed

Expression of the homeobox genes PAX6, OTX2, and OTX1 in the early human fetal retina.

OTX1 OTX2

1.81e-05386219414065
Pubmed

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

SCN1A SCN2A

1.81e-05386223859570
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

1.81e-05386218784617
Pubmed

Otx1 function overlaps with Otx2 in development of mouse forebrain and midbrain.

OTX1 OTX2

1.81e-0538629077465
Pubmed

The TINS Lecture. Understanding the roles of Otx1 and Otx2 in the control of brain morphogenesis.

OTX1 OTX2

1.81e-05386210199636
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

1.81e-05386217544618
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

1.81e-05386232845893
Pubmed

BEST1 expression in the retinal pigment epithelium is modulated by OTX family members.

OTX1 OTX2

1.81e-05386218849347
Pubmed

Identification, tissue expression, and functional characterization of Otx3, a novel member of the Otx family.

OTX1 OTX2

1.81e-05386212055180
Pubmed

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

SCN1A SCN2A

1.81e-05386228518218
Pubmed

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

SCN1A SCN2A

1.81e-05386219270815
Pubmed

CRX is a diagnostic marker of retinal and pineal lineage tumors.

OTX1 OTX2

1.81e-05386219936203
Pubmed

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

SCN1A SCN2A

1.81e-05386225155934
Pubmed

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

SCN1A SCN2A

1.81e-05386217928448
Pubmed

Association of polymorphisms in EPHX1, UGT2B7, ABCB1, ABCC2, SCN1A and SCN2A genes with carbamazepine therapy optimization.

EPHX1 SCN1A

1.81e-05386222188362
Pubmed

Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+.

GABRG2 SCN1A

1.81e-05386217927801
Pubmed

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

SCN1A SCN2A

1.81e-05386214973256
Pubmed

ABCB1 c.3435C > T and EPHX1 c.416A > G polymorphisms influence plasma carbamazepine concentration, metabolism, and pharmacoresistance in epileptic patients.

EPHX1 SCN1A

1.81e-05386234411648
Pubmed

Morphological adaptation with preserved proliferation/transporter content in the colon of patients with short bowel syndrome.

SLC9A2 SLC15A1

1.81e-05386219389806
Pubmed

Transfected beta3- but not beta2-adrenergic receptors regulate cystic fibrosis transmembrane conductance regulator activity via a new pathway involving the mitogen-activated protein kinases extracellular signal-regulated kinases.

ADRB3 CFTR

1.81e-05386215563584
Pubmed

Effects of EPHX1, SCN1A and CYP3A4 genetic polymorphisms on plasma carbamazepine concentrations and pharmacoresistance in Chinese patients with epilepsy.

EPHX1 SCN1A

1.81e-05386224125961
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

3.61e-05486217537961
Pubmed

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

SCN1A SCN2A

3.61e-05486235031483
Pubmed

Emx and Otx homeobox genes in the developing mouse brain.

OTX1 OTX2

3.61e-0548627901323
Pubmed

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

SCN1A SCN2A

3.61e-05486226637798
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

3.61e-05486229578003
Pubmed

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

SCN1A SCN2A

3.61e-05486221156207
Pubmed

Cftr and ENaC ion channels mediate NaCl absorption in the mouse submandibular gland.

SLC9A2 CFTR

3.61e-05486220026617
Pubmed

Emx1 and Emx2 show different patterns of expression during proliferation and differentiation of the developing cerebral cortex in the mouse.

OTX1 OTX2

3.61e-0548628743751
Pubmed

Conserved genetic programs in insect and mammalian brain development.

OTX1 OTX2

3.61e-05486210440864
Pubmed

A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo.

OTX1 OTX2

3.61e-0548628101484
Pubmed

Nested expression domains of four homeobox genes in developing rostral brain.

OTX1 OTX2

3.61e-0548621353865
Pubmed

Conserved homeobox genes in the developing brain.

OTX1 OTX2

3.61e-0548627915635
Pubmed

Models for discovery of targeted therapy in genetic epileptic encephalopathies.

GABRG2 SCN1A

3.61e-05486228742937
Pubmed

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

SCN1A SCN2A

3.61e-05486235801810
Pubmed

Chromosome locations of human EMX and OTX genes.

OTX1 OTX2

3.61e-0548627959790
Pubmed

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

SCN1A SCN2A

3.61e-0548628974318
Pubmed

Otx dose-dependent integrated control of antero-posterior and dorso-ventral patterning of midbrain.

OTX1 OTX2

6.01e-05586212652306
Pubmed

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

SCN1A SCN2A

6.01e-0558621679748
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

6.01e-0558628812438
Pubmed

Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila.

OTX1 OTX2

6.01e-0558627913821
Pubmed

Regulation of Otx2 expression and its functions in mouse forebrain and midbrain.

OTX1 OTX2

6.01e-05586215201224
Pubmed

MAGE-B5, MAGE-B6, MAGE-C2, and MAGE-C3: four new members of the MAGE family with tumor-specific expression.

MAGEC3 MAGEC2

6.01e-05586210861452
Pubmed

Orthopedia homeodomain protein is essential for diencephalic dopaminergic neuron development.

OTX1 OTX2

6.01e-05586217481897
Pubmed

The mouse homolog of the orphan nuclear receptor tailless is expressed in the developing forebrain.

OTX1 OTX2

6.01e-0558627720587
Pubmed

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

SCN1A SCN2A

6.01e-05586224337656
Pubmed

Murine Otx1 and Drosophila otd genes share conserved genetic functions required in invertebrate and vertebrate brain development.

OTX1 OTX2

9.01e-0568629521907
Cytoband9q31.1

OR13C9 OR13C5 OR13C3 OR13C4 OR13C2

1.46e-08418659q31.1
CytobandEnsembl 112 genes in cytogenetic band chr9q31

OR13C9 OR13C5 OR13C3 OR13C4 OR13C2

6.31e-06137865chr9q31
Cytoband2q24.3

SCN1A SCN2A

4.09e-04168622q24.3
Cytoband17q23.3

LIMD2 TEX2

1.46e-033086217q23.3
Cytoband9q33.2

PSMD5 OR1L4

2.46e-03398629q33.2
GeneFamilyOlfactory receptors, family 13

OR13C9 OR13C5 OR13C3 OR13C4 OR13C2

1.78e-0823665162
GeneFamilySodium voltage-gated channel alpha subunits

SCN1A SCN2A

4.65e-0496621203
GeneFamilyOlfactory receptors, family 8

OR8U1 OR8U9 OR8U8

7.59e-0449663155
ToppCellPCW_13-14-Neuronal-Neuronal_postreplicative-neuro_immature_neuronal_(2)|PCW_13-14 / Celltypes from embryonic and fetal-stage human lung

GABRG2 GAD2 OR2F1 CNGB1 CHRNA3

1.35e-05161845bb9cb42882aaa4a1ecf9b480c0e7ac302f2c0d5d
ToppCellPCW_13-14-Neuronal-Neuronal_postreplicative-neuro_neuronal_(6)|PCW_13-14 / Celltypes from embryonic and fetal-stage human lung

GABRG2 SCN1A SCN2A CNGB1 CHRNA3

2.26e-05179845af0b54c9ea0b6e4210f22dbb6e88ecd3276a5f86
ToppCell5'-GW_trimst-2-LargeIntestine-Neuronal-neurons_B-Branch_B1_(eMN)|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

GABRG2 LRFN5 SCN2A CNGB1 CHRNA3

2.51e-051838457e2bac8b005155888ff4b41ef2e1d975dc17abc7
ToppCellfacs-Brain_Non-Myeloid-Cerebellum-3m-Neuronal-neuron|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

GABRG2 OTX2 SCN1A SCN2A MEDAG

2.64e-0518584570de48988c1f8e0809afc8092b663aa439d8e528
ToppCell5'-GW_trimst-2-LargeIntestine-Neuronal-neurons_B|GW_trimst-2 / Celltypes from developing, pediatric, Crohn's, & adult GI tract

GABRG2 LRFN5 SCN2A CNGB1 CHRNA3

2.71e-0518684515f2e5905486e33f6f7b3b3e9758a0559e8c61ee
ToppCellfacs-Brain_Non-Myeloid-Cerebellum-3m-Neuronal|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation

GABRG2 OTX2 SCN1A SCN2A MEDAG

2.78e-051878457b2cd0c618ed081223343f3bec2244c8723c9a31
ToppCellfacs-Pancreas-Exocrine-3m-Epithelial-pancreatic_ductal_cell|Pancreas / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

EPHX1 PTPN14 GNA14 CFTR STAT4

2.85e-05188845842982de2197770f999a70083ed9fca40ac22d79
ToppCellfacs-Pancreas-Exocrine-3m-Epithelial-pancreatic_ductal_cell|Pancreas / Large_Intestine_Pancreas_Liver - method, tissue, subtissue, age, lineage, cell ontology and free annotation

EPHX1 PTPN14 GNA14 CFTR STAT4

2.85e-05188845a0815eaf68eedd6e5ec4af520df80a6ab4eb0864
ToppCellPrimary_Visual_cortex_(V1C)-Neuronal-Glutamatergic_Excit-Glut_C-D_(RORB)|Primary_Visual_cortex_(V1C) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

GABRG2 PTPN14 LRFN5 SCN1A SCN2A

3.40e-05195845787e95fb59c40bba784544b662fac37606ae1427
ToppCellCOPD-Epithelial-Club|Epithelial / Disease state, Lineage and Cell class

GNA14 GLUD1 PALS2 RNF145 ME1

3.48e-05196845af96fb94886e9395f3e2cd0a293af29229d017fe
ToppCellPrimary_Motor_Cortex_(M1)-Neuronal|Primary_Motor_Cortex_(M1) / Sample groups (6 Anatomical region groups), with 5 level hierarchy of cell types

GABRG2 LRFN5 SCN1A SCN2A PALS2

3.65e-051988454ca5ff320905ab4ff60ed90a5522227c782142a6
ToppCell5'-Parenchyma_lung-Epithelial-Alveolar_epithelium-type_II_pneumocyte-AT2-AT2_L.0.1.3.1|5' / 5'-vs-3', Tissue groups, Lineages, Lineage subclass, Cell_type2, Cell_subtype2_L4.5

ACADL SCN1A CFTR CPB2 RNF145

3.74e-051998452dc33804f6691d7c9682e6c9b885e945fb97fc36
DiseaseSeizure, Febrile, Simple

GABRG2 SCN1A SCN2A

6.92e-077813C0149886
DiseaseSeizure, Febrile, Complex

GABRG2 SCN1A SCN2A

6.92e-077813C0751057
DiseaseFebrile Convulsions

GABRG2 SCN1A SCN2A

1.65e-069813C0009952
DiseaseGeneralized Epilepsy with Febrile Seizures Plus

GABRG2 SCN1A SCN2A

1.65e-069813C3502809
Diseasegeneralized epilepsy with febrile seizures plus (implicated_via_orthology)

GABRG2 SCN1A SCN2A

4.31e-0612813DOID:0060170 (implicated_via_orthology)
DiseaseInfantile Severe Myoclonic Epilepsy

GABRG2 SCN1A SCN2A

5.59e-0613813C0751122
DiseaseFebrile seizure (within the age range of 3 months to 6 years)

GABRG2 SCN1A SCN2A

1.58e-0518813HP_0002373
DiseaseEpilepsy

GABRG2 SCN1A SCN2A GLUD1

2.36e-04109814C0014544
Diseasegeneralized epilepsy with febrile seizures plus 2 (implicated_via_orthology)

SCN1A SCN2A

3.30e-0410812DOID:0111294 (implicated_via_orthology)
DiseaseDravet syndrome (implicated_via_orthology)

SCN1A SCN2A

3.30e-0410812DOID:0080422 (implicated_via_orthology)
Diseasemiddle temporal gyrus volume measurement

OR13C3 OR13C4

4.03e-0411812EFO_0010316
Diseasechronic obstructive pulmonary disease (is_implicated_in)

EPHX1 CFTR CHRNA3

7.03e-0463813DOID:3083 (is_implicated_in)
DiseaseMMR-related febrile seizures

SCN1A SCN2A

7.64e-0415812EFO_0006519
Diseasehepatic encephalopathy (biomarker_via_orthology)

GABRG2 GLUD1

7.64e-0415812DOID:13413 (biomarker_via_orthology)
DiseaseEarly infantile epileptic encephalopathy with suppression bursts

SCN1A SCN2A

8.71e-0416812C0393706
Diseaseepilepsy (implicated_via_orthology)

GABRG2 GAD2 SCN1A SCN2A

1.07e-03163814DOID:1826 (implicated_via_orthology)
Diseaselung cancer (is_implicated_in)

MAP2K4 CFTR CHRNA3

1.12e-0374813DOID:1324 (is_implicated_in)
Diseaseanxiety disorder (implicated_via_orthology)

SCN1A SCN2A

1.66e-0322812DOID:2030 (implicated_via_orthology)
Diseaseprogranulin measurement

MAP2K4 LRFN5

1.66e-0322812EFO_0004625
DiseaseQRS duration, response to sulfonylurea

SLC15A1 LRFN5

1.81e-0323812EFO_0005055, EFO_0007922
Diseasecolorectal cancer, hormone replacement therapy

OR2F2 SLC15A1 VPS41

1.85e-0388813EFO_0003961, MONDO_0005575
DiseaseNeurodevelopmental Disorders

SCN1A SCN2A SRCAP

2.16e-0393813C1535926
Diseaseglutamine measurement

SLC38A4 GLUD1 SLC36A3

2.44e-0397813EFO_0009768
Diseaseretinitis pigmentosa (implicated_via_orthology)

CNGB1 SNRNP200

2.50e-0327812DOID:10584 (implicated_via_orthology)

Protein segments in the cluster

PeptideGeneStartEntry
LPLFIFTFLYVQMRK

CCRL2

211

O00421
PFMRLEKYVTLLQEL

ARHGEF6

376

Q15052
ILALMKTPVLFDIYE

ANXA11

266

P50995
PVIVAFIMLRAYFLQ

CFTR

1021

P13569
IPLIGEYLLFTMIFV

CHRNA3

301

P32297
LGIAFIPIILEKIMY

ABCA10

781

Q8WWZ4
FYYIMKELPQERLLI

ACADL

281

P28330
RVALKYMTPVILLVF

ADCY6

891

O43306
MQIEVFFKEIFLYIL

ARFGEF1

521

Q9Y6D6
RFMEQVVFKYLRAEP

ACTR3B

91

Q9P1U1
PLLVMLFVYARVFVV

ADRB3

216

P13945
FRAPQVMTYVREKIL

CCDC113

316

Q9H0I3
LLKHPFILMYEERAV

MAP2K4

361

P45985
AKMYVQPFRIVFLLV

RAB39A

111

Q14964
MEKILFYLFLIGIAV

LRFN5

1

Q96NI6
QELKMPLFVLFLSIY

OR8U8

21

P0C7N1
PVTLIDMDKALLYFI

GDAP2

361

Q9NXN4
PVFVLLEYVTLKKMR

GAD2

211

Q05329
YIRFEKFLPVMTEIL

EFCAB2

206

Q5VUJ9
KFLPVMTEILLERKY

EFCAB2

211

Q5VUJ9
PKLEIIFFALILVMY

OR13C4

21

Q8NGS5
FYRVLTSDIEKFMPI

ME1

86

P48163
DYFPVILKRAREFME

MAGEC2

176

Q9UBF1
YFPMIFRKAREFIEI

MAGEC3

221

Q8TD91
TVYPMERLVADKLIF

LIMD2

46

Q9BT23
YPVVVLFAMVLLDFL

OR51B6

196

Q9H340
EPKVFAIRCFKIIMY

EFR3B

266

Q9Y2G0
EFFLLIMRELLDPKY

HERC4

756

Q5GLZ8
ELIPSILEKFIRVYM

KNTC1

731

P50748
FKFLIPHIRYTMEIN

ALOX12

386

P18054
EKLFSVFYAILTPML

OR2F1

271

Q13607
PRLELLFFVLIFIMY

OR13C5

21

Q8NGS8
EKLISVFYAIVMPLL

OR2F2

271

O95006
PRLELLFFVLIFIMY

OR13C2

21

Q8NGS9
QELKMPLFVLFLSIY

OR8U9

21

P0C7N5
YRETILSKPMLFFIN

MEDAG

106

Q5VYS4
RYPDIFMREEVALKI

OTX1

61

P32242
LKVLRTSEFMPYVVF

PALS2

441

Q9NZW5
MFNRPFLVIIKEYIT

SERPINA2

391

P20848
RFMEQVIFKYLRAEP

ACTR3

91

P61158
LLYPVKEKVFYSLMR

EPHX1

281

P07099
LLRLVDFYVMPVVNV

CPB2

211

Q96IY4
FYRRAMQLVPDIEFK

FBXO9

116

Q9UK97
KLLYIRLALFFPEMV

DAGLB

96

Q8NCG7
IFLERNIMVIPDLYL

GLUD1

416

P00367
YQIEELMILLEYKIP

CNTF

121

P26441
IRIAKMDSYARIFFP

GABRG2

436

P18507
MEYVILIEFLPKYPI

CHIC1

206

Q5VXU3
ILIVIMVPIFDAVLY

SLC15A1

331

P46059
RFKMLPEVLYRIFTL

LRRC40

506

Q9H9A6
PKIEIVYFALILVMY

OR13C3

51

Q8NGS6
RYPDIFMREEVALKI

OTX2

61

P32243
KPLFAIFLIMYLLTA

OR1L4

26

Q8NGR5
TFYTFVILPKMLINL

OR10R2

91

Q8NGX6
PRLELLFFVLIFIMY

OR13C9

21

Q8NGT0
LITLDVKLQTPMYFF

OR14A2

46

Q96R54
IKVEQTLREPMFYFL

OR52J3

51

Q8NH60
QELKMPLFVLFLSIY

OR8U1

21

Q8NH10
IEYPFDLENIIFRMV

GNA14

186

O95837
LEFVIPVILVAYFNM

HRH4

181

Q9H3N8
GPFLVVRLILMTYFK

TMEM26

266

Q6ZUK4
PMVIEIIEKNFDYLR

TMEM126B

51

Q8IUX1
FIPTLVMIILYSKIF

TAAR8

206

Q969N4
PFYNVVFRRVMKLLD

PIWIL2

321

Q8TC59
VYLHKMPETDFLIIR

TAF1L

771

Q8IZX4
FLREYVLFPMDLALE

PTPN14

161

Q15678
FIIKYELPEVIRAFM

SLC38A4

171

Q969I6
ATMLIFILPAVFYLK

SLC38A4

486

Q969I6
VEQLTPIERYAMKFL

SRCAP

2306

Q6ZRS2
ILDIRFYMLIILPFL

SLC36A3

186

Q495N2
IVGMFLAELIEKYFV

SCN1A

1616

P35498
YAMVKLLLFSEVRRP

ABCB9

96

Q9NP78
MEVSFYKILQDPRLI

CIP2A

496

Q8TCG1
YTKMLFVREPFERLV

CHST8

251

Q9H2A9
IFDMLKRLRSVVYLP

CNGB1

971

Q14028
MKTDVFFLYLLPPIV

SLC9A2

136

Q9UBY0
MPYVDLRLKFLTALT

TMEM181

486

Q9P2C4
LPFADILRDYKVIMA

STAT4

636

Q14765
IVGMFLAELIEKYFV

SCN2A

1606

Q99250
LSYIKQIFPMEERIF

ZNF470

186

Q6ECI4
RLYVEVMLSFPLFKD

TSTD2

221

Q5T7W7
LKPLIYEMILHEFLE

VPS41

456

P49754
INVDDFKIIYIAPMR

SNRNP200

531

O75643
FKIIYIAPMRSLVQE

SNRNP200

536

O75643
ERYPIFVEKVFEMIE

PSMD5

291

Q16401
AERKVEVPQMFILYV

SLC9C2

396

Q5TAH2
IKLPYFMNELTLTEL

TEX2

856

Q8IWB9
YVLFMVEEFRKEPVE

RNF145

431

Q96MT1
PYSRFMIELTKLLKI

ZMYM4

1331

Q5VZL5
YKLMIFDFIIILAVT

TMC7

496

Q7Z402