5441
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Cyclic nucleotide gated channel subunit alpha 3 |
ACHM2, CCNC1, CCNCa, CCNCalpha, CNCG3, CNG3 |
Curated: Achromatopsia, Color vision deficiency, Cone dystrophy, Cone-rod dystrophy, Macular degeneration, Macular dystrophy, Optic atrophy, Retinitis pigmentosa, CNGA3-related retinopathy
Unreviewed: Atrophy, Carcinogenesis, Color Blindness, Cone Dystrophy, Cone monochromatism, Disorder Of Eye, Dyschromatopsia, Dyskinesia, Enhanced S-Cone Syndrome, Exotropia, Glioblastoma, Hemeralopia, Hyperopia, Leber Congenital Amaurosis, Macular Degeneration, Motor neuron atrophy, Myopia, Neoplasms, Night blindness, Nyctalopia, Nystagmus, Pendular nystagmus, Retinal degeneration, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Rod-cone dystrophy, Visual disorder
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5442
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Cyclic nucleotide gated channel subunit alpha 4 |
CNCA2, CNG-4, CNG4, CNG5, CNGB2, OCNC2, OCNCBETA, OCNCb |
Curated: Duodenal ulcer, Gastric ulcer, Gastroesophageal reflux disease, Peptic ulcer disease
Unreviewed: N/A
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5443
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Cyclic nucleotide gated channel subunit beta 1 |
CNCG2, CNCG3L, CNCG4, CNG4, CNGB1B, GAR1, GARP, GARP2, RCNC2, RCNCb, RCNCbeta, RP45 |
Curated: Alzheimer disease, Amblyopia, Retinitis pigmentosa, Dementia, Optic atrophy, Peripheral neuropathy, CNGB1-related retinopathy
Unreviewed: Anosmia, Arthritis, Asthma, Autoimmune Diseases, Biliary Cirrhosis, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cataract, Colorectal Cancer, Congenital abnormalities, Congenital Hypoplasia Of Penis, Coronary artery disease, Dermatitis, Developmental disability, Diabetes Mellitus, Disorder Of Eye, Eczema, Edema, Epilepsy, Glaucoma, Hearing Loss, Hepatocellular carcinoma, Hibernoma, Hyperinsulinism, Hypogonadism, Keratoconus, Liver failure, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Melanoma, Mental retardation, Microcephaly, Multiple Sclerosis, Neoplasms, Night blindness, congenital stationary, Nyctalopia, Nystagmus, Obesity, Optic Atrophy, Papillary thyroid carcinoma, Pontocerebellar hypoplasia, Retinal degeneration, Retinal detachment, Retinal Dystrophy, Retinitis Pigmentosa, Rhyns syndrome, Rod-cone dystrophy, Usher Syndrome, Visual disorder
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5444
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Cyclic nucleotide gated channel subunit beta 3 |
ACHM1 |
Curated: 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, CNGB3-related retinopathy
Unreviewed: Age-related macular degeneration, Anxiety Disorder, Cataract, Choroideremia, Color blindness, Cone Dystrophy, Cone monochromatism, Disorder Of Eye, Disorder Of Macula Of Retina, Dyschromatopsia, Exotropia, Horizontal pendular nystagmus, Hyperopia, Leber Congenital Amaurosis, Macular Degeneration, Myopia, Night blindness, congenital stationary, Nyctalopia, Pendular nystagmus, Progressive Cone Dystrophy, Retinal degeneration, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Retinitis pigmentosa inversa, Usher syndrome, Visual disorder, Vulval varices
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5445
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CNGB3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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5446
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Cornichon family member 1 |
CNIH, CNIH-1, CNIL, TGAM77 |
Curated: Colorectal cancer
Unreviewed: N/A
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5447
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Cornichon family AMPA receptor auxiliary protein 2 |
CNIH-2, Cnil |
Curated: Gout, Insomnia
Unreviewed: Diabetes Mellitus, Gouty arthritis
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5448
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Cornichon family AMPA receptor auxiliary protein 3 |
CNIH-3 |
Curated: Central nervous system cancer, Endometriosis, Glioblastoma, Glioma, Osteoarthritis, Schizophrenia
Unreviewed: Breast neoplasm, Endometrioma, Malignant Neoplasm
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5449
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CNIH3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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5450
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CNIH3 antisense RNA 2 |
- |
Curated: N/A
Unreviewed: N/A
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