Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1391 to 1400 of 1796 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1391	6775073	COX3	-	-	Spastic ataxia, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Temporal lobe epilepsy, Hearing impairment, Liver failure, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalopathy, Nephrolithiasis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy View all (4 more)
1392	8923187	COX3	-	-	Spastic ataxia, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Temporal lobe epilepsy, Hearing impairment, Liver failure, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalopathy, Nephrolithiasis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy View all (4 more)
1393	1327	COX4I1	Cytochrome c oxidase subunit 4I1	COX IV-1, COX4, COX4-1, COXIV, COXIV-1, MC4DN16	Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
1394	84701	COX4I2	Cytochrome c oxidase subunit 4I2	COX4, COX4-2, COX4B, COX4L2, COXIV-2, dJ857M17.2	Alzheimer disease, Mitochondrial disease, Pancreatic insufficiency syndrome
1395	9377	COX5A	Cytochrome c oxidase subunit 5A	COX, COX-VA, MC4DN20, VA	Alzheimer disease, Cytochrome c oxidase deficiency, Major depressive disorder, Mitochondrial complex deficiency, Myocardial infarction, Squamous cell carcinoma, Diabetes mellitus type 2
1396	1329	COX5B	Cytochrome c oxidase subunit 5B	COXVB	Myocardial ischemia
1397	1337	COX6A1	Cytochrome c oxidase subunit 6A1	CMTRID, COX6A, COX6AL	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
1398	1339	COX6A2	Cytochrome c oxidase subunit 6A2	COX6AH, COXVIAH, COXVIa-M, MC4DN18	Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease
1399	1340	COX6B1	Cytochrome c oxidase subunit 6B1	COX6B, COXG, COXVIb1, MC4DN7	Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease
1400	1345	COX6C	Cytochrome c oxidase subunit 6C	-	Lung cancer, Squamous cell carcinoma

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