Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2065
Gene Symbol: ERBB3
ERBB3 		0.600 Biomarker disease GENOMICS_ENGLAND Insulin-like Growth Factor Binding Protein-3 expression in the human corneal epithelium. 17709104 2007
Entrez Id: 2065
Gene Symbol: ERBB3
ERBB3 		0.600 GermlineCausalMutation disease ORPHANET Lethal congenital contractural syndrome type 2 (LCCS2) is caused by a mutation in ERBB3 (Her3), a modulator of the phosphatidylinositol-3-kinaseAkt pathway. 17701904 2007
Entrez Id: 2065
Gene Symbol: ERBB3
ERBB3 		0.600 Biomarker disease GENOMICS_ENGLAND Regulation of neuregulin/ErbB signaling by contractile activity in skeletal muscle. 12519750 2003
Entrez Id: 2065
Gene Symbol: ERBB3
ERBB3 		0.600 Biomarker disease CTD_human