Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2891 to 2900 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2891
Cytochrome c oxidase subunit 7C
-
Obesity

2892
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

2893
Cytochrome c oxidase associated subunit FA4
CI-9k, CI-MLRQ, MC4DN21, MISTR1, MLRQ, MRCAF1, NDUFA4
Leigh syndrome, Mitochondrial complex deficiency

2894
Cytochrome c oxidase hypoxia associated subunit FA4L2
MISTRH, NDUFA4L2, NUOMS
Rheumatoid arthritis

2895
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)

2896
Carboxypeptidase A1
CPA
Hereditary chronic pancreatitis, Pancreatitis, Diabetes mellitus type 2

2897
Carboxypeptidase A2
-
Hypoxia

2898
Carboxypeptidase A3
MC-CPA
Diverticular disease, Dyslexia, Hypertension

2899
Carboxypeptidase A4
CPA3
Color vision deficiency, Rheumatoid arthritis

2900
Carboxypeptidase A5
-
Color vision deficiency