hereditary retinal dystrophy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Similar Terms
Downloads & Tools


21 genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SPATA7 spermatogenesis associated 7 1.45001
CEP290 centrosomal protein 290kDa 1.34286
LCA5 Leber congenital amaurosis 5 1.29003
RHO rhodopsin 1.24515
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis) 1.17206
GUCY2D guanylate cyclase 2D, membrane (retina-specific) 1.06396
AIPL1 aryl hydrocarbon receptor interacting protein-like 1 1.04377
LRBA LPS-responsive vesicle trafficking, beach and anchor containing 1.01638
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1 1.0109
CRX cone-rod homeobox 0.979689
MERTK MER proto-oncogene, tyrosine kinase 0.953273
CRB1 crumbs family member 1, photoreceptor morphogenesis associated 0.876148
CKM creatine kinase, muscle 0.826589
CASP2 caspase 2, apoptosis-related cysteine peptidase 0.808129
BCKDHA branched chain keto acid dehydrogenase E1, alpha polypeptide 0.792131
RPE65 retinal pigment epithelium-specific protein 65kDa 0.709169
C1QTNF5 C1q and tumor necrosis factor related protein 5 0.566443
PRPH2 peripherin 2 (retinal degeneration, slow) 0.482464
ELOVL4 ELOVL fatty acid elongase 4 0.446182
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1 0.389281
BEST1 bestrophin 1 0.192657