Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2711 to 2720 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2711
Cyclic nucleotide gated channel subunit alpha 1
CNCG, CNCG1, CNG-1, CNG1, RCNC1, RCNCa, RCNCalpha, RP49
Colonic neoplasms, Cone-rod dystrophy, Macular dystrophy, Optic atrophy, Retinitis pigmentosa, Spondylosis

2712
Cyclic nucleotide gated channel subunit alpha 2
CNCA, CNCA1, CNG2, OCNC1, OCNCALPHA, OCNCa
Anosmia, Congenital anosmia

2713
Cyclic nucleotide gated channel subunit alpha 3
ACHM2, CCNC1, CCNCa, CCNCalpha, CNCG3, CNG3
Achromatopsia, Color vision deficiency, Cone dystrophy, Cone-rod dystrophy, Macular degeneration, Macular dystrophy, Optic atrophy, Retinitis pigmentosa

2714
Cyclic nucleotide gated channel subunit alpha 4
CNCA2, CNG-4, CNG4, CNG5, CNGB2, OCNC2, OCNCBETA, OCNCb
Duodenal ulcer, Gastric ulcer, Gastroesophageal reflux disease, Peptic ulcer disease

2715
Cyclic nucleotide gated channel subunit beta 1
CNCG2, CNCG3L, CNCG4, CNG4, CNGB1B, GAR1, GARP, GARP2, RCNC2, RCNCb, RCNCbeta, RP45
Alzheimer disease, Amblyopia, Retinitis pigmentosa, Dementia, Optic atrophy, Peripheral neuropathy

2716
Cyclic nucleotide gated channel subunit beta 3
ACHM1
Achromatopsia, Anxiety disorder, Color vision deficiency, Cone dystrophy, Cone-rod dystrophy, Leber congenital amaurosis, Macular dystrophy, Metabolic syndrome, Nystagmus, Optic atrophy, Retinitis pigmentosa, Stargardt disease, Diabetes mellitus type 2

2717
Cornichon family member 1
CNIH, CNIH-1, CNIL, TGAM77
Colorectal cancer

2718
Cornichon family AMPA receptor auxiliary protein 2
CNIH-2, Cnil
Gout, Insomnia

2719
Cornichon family AMPA receptor auxiliary protein 3
CNIH-3
Central nervous system cancer, Endometriosis, Glioblastoma, Glioma, Osteoarthritis, Schizophrenia

2720
Cornichon family member 4
CNIH-4, HSPC163
Major depressive disorder