Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1406
Gene Symbol: CRX
CRX
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness. 24382353

2014
Entrez Id: 1406
Gene Symbol: CRX
CRX
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Mechanistically distinct mouse models for CRX-associated retinopathy. 24516401

2014
Entrez Id: 1406
Gene Symbol: CRX
CRX
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice. 15676071

2005
Entrez Id: 1406
Gene Symbol: CRX
CRX
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Inner retinal abnormalities in a mouse model of Leber's congenital amaurosis. 14730587

2004
Entrez Id: 1406
Gene Symbol: CRX
CRX
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Retinopathy and attenuated circadian entrainment in Crx-deficient mice. 10581037

1999