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"
1711 to 1720 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1711
Cytochrome b5 reductase like
-
Color vision deficiency

1712
Cytochrome b-245 alpha chain
CGD4, p22-PHOX
Asthma, Atherosclerosis, Granulomatous disease, Ischemic heart disease, Obstructive airway disease, Coronary artery disease, Diabetes mellitus type 2, Hypertension, Heart disease, Hepatomegaly, Kidney failure, Liver cirrhosis, Myocardial ischemia, Oligodendroglioma

1713
Cytochrome b-245 beta chain
AMCBX2, CGD, CGDX, GP91-1, GP91-PHOX, GP91PHOX, IMD34, NOX2, p91-PHOX
Rheumatoid arthritis, Brain infarction, Bronchitis, Granulomatous disease, Ciliary dyskinesia, Congestive heart failure, Diabetes mellitus, Hypertension, Heart failure, Immunodeficiency, Kidney disease, Kidney failure, Proteinuria

1714
Cytochrome b-245 chaperone 1
C17orf62, CGD5, Eros
Granulomatous disease

1715
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

1716
Cytochrome c1
MC3DN6, UQCR4
Mitochondrial complex deficiency, Mitochondrial disease

1717
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

1718
Cytoplasmic FMR1 interacting protein 1
P140SRA-1, SHYC, SRA-1, SRA1
Eczema, Atrial septal defect, Autism, Post-traumatic stress disorder, Schizophrenia, Strabismus

1719
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

1720
Cytoglobin
HGB, NOD, STAP
Biliary cirrhosis, Cholelithiasis, Diabetic neuropathy, Hepatic insufficiency, Hepatomegaly, Liver cirrhosis, Biliary cholangitis, Retinitis pigmentosa, Diabetes mellitus type 2