Gene: ARHGAP31 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57514
Gene Symbol: ARHGAP31
ARHGAP31 		0.310 GeneticVariation disease BEFREE Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutations. 24668619 2014
Entrez Id: 57514
Gene Symbol: ARHGAP31
ARHGAP31 		0.310 GermlineCausalMutation disease ORPHANET Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies. 21565291 2011