Gene: ACTG1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.430 GeneticVariation phenotype BEFREE In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment. 19477959 2009
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.430 GeneticVariation phenotype BEFREE These findings strongly suggested that the I122V mutation in ACTG1 caused autosomal dominant non-syndromic hearing impairment in a Chinese family and expanded the spectrum of ACTG1 mutations causing hearing loss. 18804074 2008
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.430 GeneticVariation phenotype LHGDN A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26). 14684684 2003
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.430 Biomarker phenotype GENOMICS_ENGLAND FISH localization of human cytoplasmic actin genes ACTB to 7p22 and ACTG1 to 17q25 and characterization of related pseudogenes. 8941379 1996
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.430 GeneticVariation phenotype CLINVAR
Entrez Id: 71
Gene Symbol: ACTG1
ACTG1 		0.430 Biomarker phenotype HPO