Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

2841 to 2850 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2841	80219	COQ10B	Coenzyme Q10B	-	Schizophrenia
2842	27235	COQ2	Coenzyme Q2, polyprenyltransferase	CL640, COQ10D1, MSA1, PHB:PPT	Coenzyme q10 deficiency, Focal glomerulosclerosis, Kidney disease, Leigh syndrome, Mitochondrial disease, Multiple system atrophy, Nephrotic syndrome, Shy-drager syndrome, Systemic lupus erythematosus
2843	51805	COQ3	Coenzyme Q3, methyltransferase	DHHBMT, DHHBMTASE, UG0215E05, bA9819.1	Liver cirrhosis
2844	51117	COQ4	Coenzyme Q4	CGI-92, COQ10D7, SPAX10	Cerebellar ataxia, Coenzyme q10 deficiency, Developmental disability, Mitochondrial disease, Spastic ataxia
2845	84274	COQ5	Coenzyme Q5, methyltransferase	COQ10D9	Central nervous system cancer, Coenzyme q10 deficiency, Glioblastoma, Glioma, Intellectual developmental disorder, Mitochondrial disease, Neurodevelopmental disorder
2846	51004	COQ6	Coenzyme Q6, monooxygenase	CGI-10, CGI10, COQ10D6	Alzheimer disease, Coenzyme q10 deficiency, Primary coenzyme q10 deficiency
2847	10229	COQ7	Coenzyme Q7, hydroxylase	CAT5, CLK-1, CLK1, COQ10D8, HMNR9	Coenzyme q10 deficiency, Coq7-related distal hereditary motor neuropathy, Distal hereditary motor neuropathy, Primary coenzyme q10 deficiency
2848	56997	COQ8A	Coenzyme Q8A	ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9	Autosomal recessive ataxia, Cerebellar ataxia, Cataract, Cerebellar atrophy, Coenzyme q10 deficiency, Congenital neurologic anomalies, Global developmental delay, Gout, Mitochondrial disease, Nystagmus, Spinocerebellar ataxia
2849	79934	COQ8B	Coenzyme Q8B	ADCK4, NPHS9	Obstructive pulmonary disease, Crohn disease, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Inflammatory bowel disease, Mitochondrial disease, Kawasaki disease, Nephrotic syndrome, Retinitis pigmentosa, Ulcerative colitis
2850	57017	COQ9	Coenzyme Q9	C16orf49, COQ10D5	Coenzyme q10 deficiency, Leigh syndrome, Mitochondrial disease

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