Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7401
Gene Symbol: CLRN1
CLRN1
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Modeling and Preventing Progressive Hearing Loss in Usher Syndrome III. 29044151

2017
Entrez Id: 7401
Gene Symbol: CLRN1
CLRN1
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene. 22787034

2012
Entrez Id: 7401
Gene Symbol: CLRN1
CLRN1
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation. 19414487

2009