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
2871 to 2880 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2871
Coronin 7
0610011B16Rik, CRN7, POD1
Coronary artery disease, Melanoma, Prostate cancer, Schizophrenia, Diabetes mellitus type 2

2872
CORO7-PAM16 readthrough
CORO7, Coronin-7, Crn7
Chondrodysplasia, Coronary artery disease, Melanoma, Duodenitis, Gastroenteritis, Prostate cancer, Schizophrenia, Diabetes mellitus type 2

2873
Coactosin like F-actin binding protein 1
CLP
Breast neoplasms, Epilepsy, Liver cirrhosis, Hypertension

2874
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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2875
-
-
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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2876
-
-
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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2877
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10
MC4DN3
Conotruncal cardiac defect, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

2878
Cytochrome c oxidase copper chaperone COX11
COX11P, MC4DN23
Mitochondrial complex deficiency, Obsessive-compulsive disorder

2879
Cytochrome c oxidase assembly factor COX14
C12orf62, MC4DN10, PCAG1
Colorectal cancer, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease

2880
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