Gene: TYR ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7299
Gene Symbol: TYR
TYR 		0.310 Biomarker disease CTD_human Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA). 9158138 1997
Entrez Id: 7299
Gene Symbol: TYR
TYR 		0.310 Biomarker disease BEFREE Tyrosinase-negative albinism is caused only by defects in tyrosinase. 8433006 1993
Entrez Id: 7299
Gene Symbol: TYR
TYR 		0.310 Biomarker disease CTD_human Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene. 2511845 1989