Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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
2851 to 2860 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2851
Coat protein complex I subunit zeta 1
CGI-120, COPZ, HSPC181, zeta-COP, zeta1-COP
Venous thromboembolism

2852
Coat protein complex I subunit zeta 2
zeta2-COP
Bell's palsy, Osteoarthritis, Prostate cancer

2853
Coenzyme Q10A
-
Coronary artery disease, Liver cirrhosis, Psoriasis, Diabetes mellitus type 2

2854
Coenzyme Q10B
-
Schizophrenia

2855
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

2856
Coenzyme Q3, methyltransferase
DHHBMT, DHHBMTASE, UG0215E05, bA9819.1
Liver cirrhosis

2857
Coenzyme Q4
CGI-92, COQ10D7, SPAX10
Cerebellar ataxia, Coenzyme q10 deficiency, Developmental disability, Mitochondrial disease, Spastic ataxia

2858
Coenzyme Q5, methyltransferase
COQ10D9
Central nervous system cancer, Coenzyme q10 deficiency, Glioblastoma, Glioma, Intellectual developmental disorder, Mitochondrial disease, Neurodevelopmental disorder

2859
Coenzyme Q6, monooxygenase
CGI-10, CGI10, COQ10D6
Alzheimer disease, Coenzyme q10 deficiency, Primary coenzyme q10 deficiency

2860
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