Anhydrotic Ectodermal Dysplasias Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1706004
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Genes

29 genes associated with the disease Anhydrotic Ectodermal Dysplasias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BMS1 BMS1 ribosome biogenesis factor
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CXCR4 chemokine (C-X-C motif) receptor 4
EDA ectodysplasin A
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain
EFNB1 ephrin-B1
ELANE elastase, neutrophil expressed
GFI1 growth factor independent 1 transcription repressor
GH1 growth hormone 1
GJB6 gap junction protein, beta 6, 30kDa
HAND2 heart and neural crest derivatives expressed 2
IFNG interferon, gamma
IFNGR1 interferon gamma receptor 1
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
ITGB4 integrin, beta 4
LEF1 lymphoid enhancer-binding factor 1
MADCAM1 mucosal vascular addressin cell adhesion molecule 1
NFKBIA nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
NR4A3 nuclear receptor subfamily 4, group A, member 3
ORAI1 ORAI calcium release-activated calcium modulator 1
RHOA ras homolog family member A
STAT1 signal transducer and activator of transcription 1, 91kDa
STIM1 stromal interaction molecule 1
TAB2 TGF-beta activated kinase 1/MAP3K7 binding protein 2
TNF tumor necrosis factor
TP63 tumor protein p63
TRAF6 TNF receptor-associated factor 6, E3 ubiquitin protein ligase
WNT10A wingless-type MMTV integration site family, member 10A