Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3211 to 3220 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3211
Cytochrome b5 reductase 4
NCB5OR, cb5/cb5R, dJ676J13.1
Diabetes mellitus type 2, Lewy body disease, Ocular sarcoidosis, Oligodendroglioma

3212
Cytochrome b5 reductase like
-
Color vision deficiency

3213
Cytochrome b-245 alpha chain
CGD4, p22-PHOX
Asthma, Atherosclerosis, Granulomatous disease, Ischemic heart disease, Obstructive airway disease, Coronary artery disease, Experimental diabetes, Diabetes mellitus type 2, Hypertension, Heart disease, Hepatomegaly, Kidney failure, Liver cirrhosis, Myocardial ischemia, Oligodendroglioma

3214
Cytochrome b-245 beta chain
AMCBX2, CGD, CGDX, GP91-1, GP91-PHOX, GP91PHOX, IMD34, NOX2, p91-PHOX
Rheumatoid arthritis, Atypical mycobacteriosis, Brain infarction, Bronchitis, Granulomatous disease, Ciliary dyskinesia, Congestive heart failure, Diabetes mellitus, Experimental diabetes, Hypertension, Heart failure, Immunodeficiency, Kidney disease, Kidney failure, Liver cirrhosis
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3215
Cytochrome b-245 chaperone 1
C17orf62, CGD5, Eros
Granulomatous disease

3216
Cytochrome b reductase 1
CYB561A2, DCYTB, FRRS3
Asthma, Breast cancer, Cancer, Colorectal cancer, Dementia, Estrogen-receptor negative breast cancer, Hereditary hemochromatosis, Lung cancer, Metabolic syndrome, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma, Diabetes mellitus type 2

3217
Cytochrome c1
MC3DN6, UQCR4
Mitochondrial complex deficiency, Mitochondrial disease

3218
Cytochrome c, somatic
CYC, HCS, THC4
Alzheimer disease, Thrombocytopenia with normal platelets, Brain ischemia, Chloracne, Fatty liver, Fatty liver, alcoholic, Methylmalonic acidemia, Obesity, Systemic lupus erythematosus, Thrombocytopenia, Transient ischemic attack

3219
Cytoplasmic FMR1 interacting protein 1
P140SRA-1, SHYC, SRA-1, SRA1
Eczema, Atrial septal defect, Autism, Post-traumatic stress disorder, Schizophrenia, Strabismus

3220
Cytoplasmic FMR1 interacting protein 2
DEE65, EIEE65, PIR121
Asthma, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Respiratory system disease