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 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

931
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

932
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)

933
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

934
Coiled-coil-helix-coiled-coil-helix domain containing 2
C7orf17, MIX17B, MNRR1, NS2TP, PARK22
Dementia, Parkinson disease

935
Coiled-coil-helix-coiled-coil-helix domain containing 3
MICOS19, MINOS3, Mic19, PPP1R22
Insomnia

936
Coiled-coil-helix-coiled-coil-helix domain containing 5
C2orf9, CHTM1, MIC14, MIX14
Amenorrhea, Dental caries, Dental enamel hypoplasia, Tooth agenesis

937
Coiled-coil-helix-coiled-coil-helix domain containing 6
CHCM1, MICOS25, Mic25, PPP1R23
Diabetic maculopathy, Squamous cell carcinoma

938
Coiled-coil-helix-coiled-coil-helix domain containing 7
COX23
Basal cell carcinoma, Cervical cancer, Scoliosis

939
Chromodomain helicase DNA binding protein 1
CHD-1, PILBOS
Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Neurodevelopmental disorder, Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome, Intellectual developmental disorder autism speech dysmorphic, Memory disorders, Non-specific syndromic intellectual disability, Prostatic neoplasms

940
Chromodomain helicase DNA binding protein 1 like
ALC1, CHDL
Congenital anomalies of the kidney and urinary tract, Congenital anomalies of kidney and urinary tract, Diabetes mellitus type 2