Genes?

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?All genes including those with curated and unreviewed disease associations.
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Chromosome:
Gene type:
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Showing genes starting with "C"
2681 to 2690 of 3566 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2681
Cytochrome c oxidase subunit 5B pseudogene 8
-

Curated: N/A

Unreviewed: N/A

2682
Cytochrome c oxidase subunit 6A1
CMTRID, COX6A, COX6AL

Curated: Androgenetic alopecia, Charcot-marie-tooth disease, Basal cell carcinoma, Bipolar disorder, Breast cancer, Dejerine-sottas disease, Dyslexia, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Mitochondrial disease, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Specific language disorder

Unreviewed: Carcinogenesis, Charcot-Marie-Tooth Disease, Cytochrome-C Oxidase Deficiency, Hereditary spastic paraplegia, Peripheral nervous system disease, Peripheral Neuropathy

2683
COX6A1 pseudogene 1
COX6A1P

Curated: N/A

Unreviewed: N/A

2684
COX6A1 pseudogene 2
-

Curated: N/A

Unreviewed: N/A

2685
COX6A1 pseudogene 3
-

Curated: N/A

Unreviewed: N/A

2686
COX6A1 pseudogene 4
-

Curated: N/A

Unreviewed: N/A

2687
COX6A1 pseudogene 5
-

Curated: N/A

Unreviewed: N/A

2688
COX6A1 pseudogene 6
-

Curated: N/A

Unreviewed: N/A

2689
COX6A1 pseudogene 7
-

Curated: N/A

Unreviewed: N/A

2690
Cytochrome c oxidase subunit 6A2
COX6AH, COXVIAH, COXVIa-M, MC4DN18

Curated: Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease

Unreviewed: Alzheimer disease, Breast neoplasm, Cytochrome-C Oxidase Deficiency, Esophageal neoplasm, Hepatocellular carcinoma, Isolated Cytochrome C Oxidase Deficiency, Ventricular remodeling