Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2421 to 2430 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2421
Cell growth regulator with EF-hand domain 1
CGR11
Attention deficit hyperactivity disorder, Fructokinase deficiency, Liver neoplasms, Post-traumatic stress disorder, Diabetes mellitus type 2, Vascular dementia

2422
Cell growth regulator with ring finger domain 1
CGR19, RNF197
Prostate cancer

2423
Cholesterol 25-hydroxylase
C25H
Crohn disease, Heart failure, Inflammatory bowel disease, Ulcerative colitis

2424
ChaC glutathione specific gamma-glutamylcyclotransferase 1
-
Hypertension

2425
Chondroadherin like
SLRR4B
Major depressive disorder, Migraine, Osteoarthritis

2426
Chromatin assembly factor 1 subunit A
CAF-1, CAF1, CAF1B, CAF1P150, P150
Goldenhar syndrome, Systemic lupus erythematosus, Mouth disease

2427
Chromatin assembly factor 1 subunit B
CAF-1, CAF-IP60, CAF1, CAF1A, CAF1P60, MPHOSPH7, MPP7
Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Global developmental delay, Hypertension, Intellectual developmental disorder, Mouth disease

2428
Chromosome alignment maintaining phosphoprotein 1
C13orf8, CAMP, CHAMP, MRD40, NEDHILD, ZNF828
Nonsyndromic intellectual disability, Neurodevelopmental disorder, Hypertension, Intellectual developmental disorder, Non-specific syndromic intellectual disability

2429
Choline O-acetyltransferase
CHOACTASE, CMS1A, CMS1A2, CMS6
Alzheimer disease, Angle closure glaucoma, Autism, Presynaptic congenital myasthenic syndromes, Congenital myasthenic syndrome, Major depressive disorder, Diabetic neuropathy, Febrile convulsion, Glaucoma, Hodgkin lymphoma, Myasthenic syndrome, Presynaptic congenital myasthenic syndrome, Prostate cancer, Schizophrenia, Seizures
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2430
Coiled-coil-helix-coiled-coil-helix domain containing 10
C22orf16, FTDALS2, IMMD, MIX17A, N27C7-4, SMAJ
Amyotrophic lateral sclerosis, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Frontotemporal dementia with motor neuron disease, Mitochondrial disease, Spinal muscular atrophy