Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
931 to 940 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

931
Cell growth regulator with ring finger domain 1
CGR19, RNF197
Prostate cancer

932
Cholesterol 25-hydroxylase
C25H
Crohn disease, Heart failure, Inflammatory bowel disease, Ulcerative colitis

933
ChaC glutathione specific gamma-glutamylcyclotransferase 1
-
Hypertension

934
Chondroadherin like
SLRR4B
Major depressive disorder, Migraine, Osteoarthritis

935
Chromatin assembly factor 1 subunit A
CAF-1, CAF1, CAF1B, CAF1P150, P150
Goldenhar syndrome, Systemic lupus erythematosus, Mouth disease

936
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

937
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

938
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
View all (2 more)

939
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

940
Coiled-coil-helix-coiled-coil-helix domain containing 2
C7orf17, MIX17B, MNRR1, NS2TP, PARK22
Dementia, Parkinson disease