Congenital Hemihypertrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0332890
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Genes

19 genes associated with the disease Congenital Hemihypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
AFP alpha-fetoprotein
AKT1 v-akt murine thymoma viral oncogene homolog 1
AKT2 v-akt murine thymoma viral oncogene homolog 2
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
FOXF1 forkhead box F1
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
HRAS Harvey rat sarcoma viral oncogene homolog
IGF2 insulin-like growth factor 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KRAS Kirsten rat sarcoma viral oncogene homolog
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PITX2 paired-like homeodomain 2
PTEN phosphatase and tensin homolog
RNF125 ring finger protein 125, E3 ubiquitin protein ligase
SMPD1 sphingomyelin phosphodiesterase 1, acid lysosomal
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
WT1 Wilms tumor 1