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"
1401 to 1410 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1401
Cytochrome c oxidase subunit 7A2
COX7AL, COX7AL1, COXVIIAL, COXVIIa-L, VIIAL
Asthma

1402
Cytochrome c oxidase subunit 7A2 like
COX7AR, COX7RP, EB1, SCAF1, SCAFI, SIG81
Colorectal cancer, Gastroesophageal reflux disease, Stroke, Venous thromboembolism

1403
Cytochrome c oxidase subunit 7B
APLCC, LSDMCA2
Microphthalmia

1404
Cytochrome c oxidase subunit 7B2
-
Alzheimer disease, Hepatocellular carcinoma, Migraine

1405
Cytochrome c oxidase subunit 7C
-
Obesity

1406
Cytochrome c oxidase subunit 8A
COX, COX8, COX8-2, COX8L, MC4DN15, VIII, VIII-L
Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

1407
Cytochrome c oxidase associated subunit FA4
CI-9k, CI-MLRQ, MC4DN21, MISTR1, MLRQ, MRCAF1, NDUFA4
Leigh syndrome, Mitochondrial complex deficiency

1408
Cytochrome c oxidase hypoxia associated subunit FA4L2
MISTRH, NDUFA4L2, NUOMS
Rheumatoid arthritis

1409
Ceruloplasmin
AB073614, CP-2
Aceruloplasminemia, Rheumatoid arthritis, Ataxia, Autism, Brain disease, Hepatocellular carcinoma, Colonic neoplasms, Ferroxidase deficiency, Dementia, Diabetes mellitus, Diabetes mellitus type 1, Iron metabolism disorder, Dyskinesia, Epilepsy, Apoceruloplasmin deficiency
View all (13 more)

1410
Carboxypeptidase A1
CPA
Hereditary chronic pancreatitis, Pancreatitis, Diabetes mellitus type 2