Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3201 to 3210 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3201
Cytochrome b561
CGCytb, CYB561A1, FRRS2, ORTHYP2
Alzheimer disease, Cardiovascular disease, Hypertension, Schizophrenia

3202
Cytochrome b561 family member A3
CYBASC3, LCYTB
Aplasia of the vermis

3203
Cytochrome b561 family member D1
-
Dyslexia, Obesity, Schizophrenia

3204
Cytochrome b561 family member D2
101F6, TSCytb, TSP10, XXcos-LUCA11.4
Cerebellar atrophy with seizures and variable developmental delay, Insomnia

3205
Cytochrome b5 type A
CYB5, MCB5, METAG
46, xy disorder of sex development, Duchenne muscular dystrophy, Endometriosis, Methemoglobinemia, Obesity

3206
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

3207
Cytochrome b5 domain containing 2
-
Central nervous system cancer, Glioblastoma, Glioma, Diabetes mellitus type 2

3208
Cytochrome b5 reductase 1
B5R.1, B5R1, B5R2, NQO3A2, humb5R2
Colorectal cancer

3209
Cytochrome b5 reductase 2
B5R.2
Contracture

3210
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