Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10951 to 10960 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10951
RCSD domain containing 1
CAPZIP, MK2S4
Appendicitis, Astrocytoma, Central nervous system cancer, Kidney disease, Color vision deficiency, Glioma, Kidney failure, Sarcoidosis

10952
RD3 regulator of GUCY2D
C1orf36, LCA12
Asthma, Kidney disease, Hypertension, Kidney failure, Leber congenital amaurosis, Lung cancer, Retinitis pigmentosa, Retinopathy, Squamous cell carcinoma

10953
Retinol dehydrogenase 10
SDR16C4
Craniofacial abnormalities

10954
Retinol dehydrogenase 11
ARSDR1, CGI82, HCBP12, MDT1, PSDR1, RALR1, RDJCSS, SCALD, SDR7C1
Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome, Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome

10955
Retinol dehydrogenase 12
LCA13, RP53, SDR7C2
Cone-rod dystrophy, Leber congenital amaurosis, Macular dystrophy, Optic atrophy, Leber hereditary optic neuropathy, Retinal degeneration, Retinitis pigmentosa, Stargardt disease

10956
Retinol dehydrogenase 13
SDR7C3
Aortic disease, Necrosis

10957
Retinol dehydrogenase 14
PAN2, SDR7C4
Cerebellar atrophy, Gout, Intellectual developmental disorder, Colorectal adenoma, Oligodendroglioma, Peptic ulcer disease, Diabetes mellitus type 2

10958
Retinol dehydrogenase 16
RODH-4, RODH4, SDR9C8, hRDH-E
Insomnia, Migraine, Respiratory system disease, Diabetes mellitus type 2

10959
Retinol dehydrogenase 5
9cRDH, HSD17B9, RDH1, SDR9C5
Atrial fibrillation, Atrophic macular degeneration, Macular and posterior pole degeneration, Eye disease, Hyperopia, Macular degeneration, Myopia, Night blindness, congenital stationary, Optic atrophy, Retinal detachment, Retinitis pigmentosa, Retinitis punctata albescens, Retinopathy, Age-related macular degeneration

10960
Retinol dehydrogenase 8
PRRDH, SDR28C2, STGD5
Cardiovascular disease, Corneal degeneration, Keratoconus, Stargardt disease