Abnormality Of Prenatal Development Or Birth Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the fetus or the birth of the fetus, excluding structural abnormalities. (Human Phenotype Ontology, HP_0001197)
External Link https://www.disgenet.org/browser/0/1/0/C4025797
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Genes

23 genes associated with the disease Abnormality Of Prenatal Development Or Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKAP9 A kinase (PRKA) anchor protein 9
ANK2 ankyrin 2, neuronal
CALM1 calmodulin 1 (phosphorylase kinase, delta)
CALM2 calmodulin 2 (phosphorylase kinase, delta)
CAV3 caveolin 3
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
ERCC2 excision repair cross-complementation group 2
ERCC3 excision repair cross-complementation group 3
GTF2E2 general transcription factor IIE, polypeptide 2, beta 34kDa
GTF2H5 general transcription factor IIH, polypeptide 5
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MPLKIP M-phase specific PLK1 interacting protein
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
RNF113A ring finger protein 113A
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN4B sodium channel, voltage gated, type IV beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SNTA1 syntrophin, alpha 1
TRDN triadin