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"
1271 to 1280 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1271
Centriolin
CEP1, CEP110, FAN, bA165P4.1
Breast cancer, Prostate cancer, Urticaria, Vitreous body disease

1272
Centrobin, centriole duplication and spindle assembly protein
LIP8, PP1221
Oligodendroglioma, Polycystic ovary syndrome, Polycythemia, Psoriasis

1273
Cytochrome c oxidase assembly factor 1
C7orf44, MITRAC15
Patellar tendinitis

1274
Cytochrome c oxidase assembly factor 3
CCDC56, COX25, HSPC009, MC4DN14, MITRAC12, hCOA3
Basal cell carcinoma, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease

1275
Cytochrome c oxidase assembly factor 5
6330578E17Rik, C2orf64, CEMCOX3, MC4DN9, Pet191
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Central nervous system cancer, Cytochrome c oxidase deficiency, Glioma, Mitochondrial complex deficiency

1276
Cytochrome c oxidase assembly factor 6
C1orf31, CEMCOX4, MC4DN13
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency

1277
Cytochrome c oxidase assembly factor 7
C1orf163, RESA1, SCAN3, SELRC1
Basal cell carcinoma, Mitochondrial disease, Spinocerebellar ataxia

1278
Cytochrome c oxidase assembly factor 8
APOP, APOP1, APOPT1, C14orf153, MC4DN17
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Breast cancer, Insomnia, Major depressive disorder, Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Obsessive-compulsive disorder, Schizophrenia

1279
Coenzyme A synthase
DPCK, NBIA6, NBP, PCH12, PPAT, UKR1, pOV-2
Coasy protein-associated neurodegeneration, Coenzyme a synthase protein associated neurodegeneration, Hallervorden spatz syndrome, Metabolic syndrome, Mucopolysaccharidosis, Neurodegeneration with brain iron accumulation, Pontocerebellar hypoplasia, Diabetes mellitus type 2

1280
Cordon-bleu WH2 repeat protein
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Autoimmune disease, Central nervous system cancer, Chromosomal disorder, Glioblastoma, Glioma, Major depressive disorder, Nasal disorder, Oligodendroglioma, Osteoarthritis, Squamous cell carcinoma, Diabetes mellitus type 1, Diabetes mellitus type 2, Vascular disease