Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
1701 to 1710 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1701
Cytochrome b561 family member A3
CYBASC3, LCYTB
Aplasia of the vermis

1702
Cytochrome b561 family member D1
-
Dyslexia, Obesity, Schizophrenia

1703
Cytochrome b561 family member D2
101F6, TSCytb, TSP10, XXcos-LUCA11.4
Cerebellar atrophy with seizures and variable developmental delay, Insomnia

1704
Cytochrome b5 type A
CYB5, MCB5, METAG
46,xy disorder of sex developmen, Duchenne muscular dystrophy, Endometriosis, Methemoglobinemia, Obesity

1705
Cytochrome b5 type B
CYB5-M, CYPB5M, OMB5
Cardiovascular disease, Cataract, Cholecystolithiasis, Coronary artery disease, Diabetes mellitus, Gallstones, Gout, Heart failure, Metabolic syndrome, Osteoarthritis, Peripheral arterial disease, Peripheral vascular disease, Diabetes mellitus type 2, Vascular disease

1706
Cytochrome b5 domain containing 2
-
Central nervous system cancer, Glioblastoma, Glioma, Diabetes mellitus type 2

1707
Cytochrome b5 reductase 1
B5R.1, B5R1, B5R2, NQO3A2, humb5R2
Colorectal cancer

1708
Cytochrome b5 reductase 2
B5R.2
Contracture

1709
Cytochrome b5 reductase 3
B5R, DIA1
Congenital myopathy, Congenital methemoglobinemia, Cyanosis, Cytochrome-b5 reductase deficiency, Dihydrolipoamide dehydrogenase deficiency, Intellectual developmental disorder, Methemoglobinemia, Osteoarthritis, Scoliosis, Diabetes mellitus type 2, Venous thromboembolism

1710
Cytochrome b5 reductase 4
NCB5OR, cb5/cb5R, dJ676J13.1
Diabetes mellitus type 2, Lewy body disease, Ocular sarcoidosis, Oligodendroglioma