Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6101
Gene Symbol: RP1
RP1
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.200 Biomarker MGD A murine RP1 missense mutation causes protein mislocalization and slowly progressive photoreceptor degeneration. 25088982

2014

Entrez Id: 6101
Gene Symbol: RP1
RP1
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.200 Biomarker MGD Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa. 19657028

2009

Entrez Id: 6101
Gene Symbol: RP1
RP1
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.200 Biomarker MGD The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein. 15269252

2004

Entrez Id: 6101
Gene Symbol: RP1
RP1
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
0.200 Biomarker MGD Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene. 11960024

2002