Disease table of SEIZURES, BENIGN FAMILIAL INFANTILE OMIM ID: PS601764

Gene-disease associations table

GeneAssociated with SEIZURES, BENIGN FAMILIAL INFANTILE inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
SCN2AClinVar, OMIM, HUMSAVARHGNC link2q24.32PS308350, PS601764
PRRT2ClinVar, OMIM, HUMSAVARHGNC link16p11.23602066, PS128100, PS601764

Download the disease annotation in CSV format

Relations among genes:

Tandem repeat annotations from DGD
Cytogenetic band analysis
Transcription Factors (TF) annotation from TRRUST
Interactions from BIOGRID - physical
Interactions from BIOGRID - genetic
Interactions from STRING
Interactions from CORUM
Interactions from CENSUS
Interactions from PDB
Interactions from manually curated literature
KEGG pathways annotation: shared terms / NET-GE enrichment (no shared terms)
REACTOME pathways annotation: shared terms / NET-GE enrichment (no shared terms)
GO - molecular function annotation: shared terms / NET-GE enrichment (no shared terms)
GO - biological process annotation: shared terms (no NET-GE enrichment)

Shared terms

GOICNumber of genes with the same GOGenes
response to stimulus (GO:0050896) 1.222PRRT2, SCN2A
GO - cellular component annotation: shared terms (no NET-GE enrichment)

Shared terms

GOICNumber of genes with the same GOGenes
integral component of membrane (GO:0016021) 1.142PRRT2, SCN2A
membrane (GO:0016020) 0.682PRRT2, SCN2A
cell part (GO:0044464) 0.112PRRT2, SCN2A
intrinsic component of membrane (GO:0031224) 1.132PRRT2, SCN2A
plasma membrane (GO:0005886) 1.392PRRT2, SCN2A
membrane part (GO:0044425) 0.952PRRT2, SCN2A
cell junction (GO:0030054) 2.752PRRT2, SCN2A