GJA8, gap junction protein alpha 8, 2703

N. diseases: 82; N. variants: 21
Disease: Multiple congenital anomalies ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		0.100 GeneticVariation group CLINVAR Exome sequencing identifies a novel mutation in GJA8 associated with inherited cataract in a Chinese family. 27785597 2017
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		0.100 GeneticVariation group CLINVAR Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing. 26694549 2016
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		0.100 GeneticVariation group CLINVAR A novel mutation in GJA8 causing congenital cataract-microcornea syndrome in a Chinese pedigree. 20806042 2010