Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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

Showing genes starting with "C"

1361 to 1370 of 1806 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1361	51226	COPZ2	Coat protein complex I subunit zeta 2	zeta2-COP	Bell's palsy, Osteoarthritis, Prostate cancer
1362	93058	COQ10A	Coenzyme Q10A	-	Coronary artery disease, Liver cirrhosis, Psoriasis, Diabetes mellitus type 2
1363	80219	COQ10B	Coenzyme Q10B	-	Schizophrenia
1364	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
1365	51805	COQ3	Coenzyme Q3, methyltransferase	DHHBMT, DHHBMTASE, UG0215E05, bA9819.1	Liver cirrhosis
1366	51117	COQ4	Coenzyme Q4	CGI-92, COQ10D7, SPAX10	Cerebellar ataxia, Coenzyme q10 deficiency, Developmental disability, Mitochondrial disease, Spastic ataxia
1367	84274	COQ5	Coenzyme Q5, methyltransferase	COQ10D9	Central nervous system cancer, Coenzyme q10 deficiency, Glioblastoma, Glioma, Intellectual developmental disorder, Mitochondrial disease, Neurodevelopmental disorder
1368	51004	COQ6	Coenzyme Q6, monooxygenase	CGI-10, CGI10, COQ10D6	Alzheimer disease, Coenzyme q10 deficiency, Primary coenzyme q10 deficiency
1369	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
1370	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

«««...135 136137138 139...»»»