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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5761 to 5770 of 193650 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

5761
COX6A1 pseudogene 1
COX6A1P

Curated: N/A

Unreviewed: N/A

5762
COX6A1 pseudogene 2
-

Curated: N/A

Unreviewed: N/A

5763
COX6A1 pseudogene 3
-

Curated: N/A

Unreviewed: N/A

5764
COX6A1 pseudogene 4
-

Curated: N/A

Unreviewed: N/A

5765
COX6A1 pseudogene 5
-

Curated: N/A

Unreviewed: N/A

5766
COX6A1 pseudogene 6
-

Curated: N/A

Unreviewed: N/A

5767
COX6A1 pseudogene 7
-

Curated: N/A

Unreviewed: N/A

5768
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

5769
Cytochrome c oxidase subunit 6B1
COX6B, COXG, COXVIb1, MC4DN7

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

Unreviewed: Anemia, Cardiomyopathy, Colorectal neoplasm, Cytochrome-C Oxidase Deficiency, Developmental Delay, Fanconi syndrome, Hearing Loss, Heart disease, High palate, Hydrocephalus, Hypertrophic cardiomyopathy, Isolated Cytochrome C Oxidase Deficiency, Leukoencephalopathy, Lymphatic metastasis, Mental retardation, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Motor delay, Optic Atrophy, Phosphate Diabetes, Ptosis, Renal Carcinoma, Renal Tubular Disorder, Retinitis Pigmentosa, Squamous cell carcinoma

5770
Cytochrome c oxidase subunit 6B1 pseudogene 1
COX6BP-1, COX6BP1

Curated: N/A

Unreviewed: N/A