Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
2751 to 2760 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2751
Cytochrome c oxidase assembly factor 1
C7orf44, MITRAC15
Patellar tendinitis

2752
Cytochrome c oxidase assembly factor 3
CCDC56, COX25, HSPC009, MC4DN14, MITRAC12, hCOA3
Basal cell carcinoma, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease

2753
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

2754
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

2755
Cytochrome c oxidase assembly factor 7
C1orf163, RESA1, SCAN3, SELRC1
Basal cell carcinoma, Mitochondrial disease, Spinocerebellar ataxia

2756
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

2757
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

2758
Cordon-bleu WH2 repeat protein
-
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

2759
Cordon-bleu WH2 repeat protein like 1
COBLR1
Cleft lip and palate, Coronary artery disease, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Hyperlipidemia, Gout, Metabolic syndrome, Myocardial ischemia, Nonalcoholic fatty liver disease, Psoriasis, Diabetes mellitus type 2, Diabetic nephropathy type 2, Uterine fibroid

2760
Cochlin
COCH-5B2, COCH5B2, DFNA9, DFNB110
Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital hearing disorder, Deafness, Esophageal adenocarcinoma, Hearing impairment, Hearing loss, Hereditary hearing loss, Hypertension, Nephrotic syndrome, Usher syndrome