Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
481 to 490 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
C-X3-C motif chemokine receptor 1
CCRL1, CMKBRL1, CMKDR1, GPR13, GPRV28, V28
Asthma, Autoimmune thyroid disease, Coronary artery disease, Human immunodeficiency virus infection, Hypothyroidism, Macular degeneration, Obesity, Psoriasis, Retinal degeneration, Systemic sclerosis

482
Cytochrome b5 type A
CYB5, MCB5, METAG
46,xy disorder of sex development, Duchenne muscular dystrophy, Endometriosis, Methemoglobinemia, Obesity

483
CREB3 regulatory factor
C5orf41, LRF
Dyslexia, Paroxysmal tachycardia

484
Centrosomal protein 120
CCDC100, JBTS31, SRTD13
Jeune syndrome, Atrial fibrillation, Breast cancer, Ciliopathies, Coronary artery disease, Desbuquois syndrome, Erythrocytosis, Aplasia of the vermis, Joubert syndrome, Jervell and lange-nielsen syndrome, Jeune thoracic dystrophy, Metabolic syndrome, Multiple myeloma, Obesity, Prostate cancer
View all (4 more)

485
Cytochrome b561
CGCytb, CYB561A1, FRRS2, ORTHYP2
Alzheimer disease, Cardiovascular disease, Hypertension, Schizophrenia

486
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

487
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, Diabetes mellitus, Experimental diabetes, Hypertension, Heart failure, Immunodeficiency, Kidney disease, Kidney failure, Liver cirrhosis, Proteinuria
View all (1 more)

488
Cytochrome c1
MC3DN6, UQCR4
Mitochondrial complex deficiency, Mitochondrial disease

489
CYLD lysine 63 deubiquitinase
BRSS, CDMT, CYLD1, CYLDI, EAC, FTDALS8, MFT, MFT1, SBS, TEM, USPL2
Amyotrophic lateral sclerosis, Asthma, Brooke-spiegler syndrome, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Crohn disease, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Leprosy, Multiple familial trichoepithelioma, Ulcerative colitis, Uterine fibroid

490
CNKSR family member 3
CNK3, CNK3/IPCEF1, MAGI1
Color vision deficiency, Osteonecrosis of the femoral head, Parkinson disease