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
2861 to 2870 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2861
Mitochondrially encoded cytochrome c oxidase I
COI, MTCO1
Carcinoma, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Hypertrophy, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Leber hereditary optic neuropathy, Rod-cone dystrophy
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2862
-
-
Carcinoma, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Hypertrophy, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Leber hereditary optic neuropathy, Rod-cone dystrophy
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2863
-
-
Carcinoma, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Hypertrophy, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Leber hereditary optic neuropathy, Rod-cone dystrophy
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2864
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
MC4DN3
Conotruncal cardiac defect, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

2865
Cytochrome c oxidase copper chaperone COX11
COX11P, MC4DN23
Mitochondrial complex deficiency, Obsessive-compulsive disorder

2866
Cytochrome c oxidase assembly factor COX14
C12orf62, MC4DN10, PCAG1
Colorectal cancer, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease

2867
Cytochrome c oxidase assembly factor COX15
CEMCOX2, HAS, MC4DN6
Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cardiomyopathy, Cytochrome c oxidase deficiency, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

2868
Cytochrome c oxidase assembly factor COX16
C14orf112, HSPC203, MC4DN22, hCOX16
Mitochondrial complex deficiency, Obsessive-compulsive disorder, Prostate cancer

2869
Cytochrome c oxidase copper chaperone COX17
-
Lung neoplasms

2870
Cytochrome c oxidase assembly factor COX18
COX18HS, OXA1L2
Mitochondrial complex deficiency, Hearing loss