Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1711 to 1720 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1711
Cytochrome b561 family member A3
CYBASC3, LCYTB
Aplasia of the vermis

1712
Cytochrome b561 family member D1
-
Dyslexia, Obesity, Schizophrenia

1713
Cytochrome b561 family member D2
101F6, TSCytb, TSP10, XXcos-LUCA11.4
Cerebellar atrophy with seizures and variable developmental delay, Insomnia

1714
Cytochrome b5 type A
CYB5, MCB5, METAG
46, xy disorder of sex development, Duchenne muscular dystrophy, Endometriosis, Methemoglobinemia, Obesity

1715
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

1716
Cytochrome b5 domain containing 2
-
Central nervous system cancer, Glioblastoma, Glioma, Diabetes mellitus, type 2

1717
Cytochrome b5 reductase 1
B5R.1, B5R1, B5R2, NQO3A2, humb5R2
Colorectal cancer

1718
Cytochrome b5 reductase 2
B5R.2
Contracture

1719
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

1720
Cytochrome b5 reductase 4
NCB5OR, cb5/cb5R, dJ676J13.1
Diabetes mellitus type 2, Lewy body disease, Ocular sarcoidosis, Oligodendroglioma