Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1011 to 1020 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1011
C-X-C motif chemokine receptor 4
CD184, D2S201E, FB22, HM89, HSY3RR, LAP-3, LAP3, LCR1, LESTR, NPY3R, NPYR, NPYRL, NPYY3R, WHIM, WHIMS, WHIMS1
Juvenile arthritis, Rheumatoid arthritis, Breast neoplasm, Juvenile idiopathic arthritis, Multiple sclerosis, Myeloproliferative disorder, Nephrosclerosis, Osteoporosis, Oligoarticular juvenile idiopathic arthritis, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Whim syndrome

1012
CRELD disulfide isomerase 1
AVSD2, CIRRIN, JELANS
Atrioventricular septal defect, Neurodevelopmental disorder, Congenital heart disease, Congenital hyperammonemia, Non-specific syndromic intellectual disability, Partial atrioventricular canal defect, Ventricular septal defect

1013
Collectin subfamily member 11
3MC2, CL-11, CL-K1-I, CL-K1-II, CL-K1-IIa, CL-K1-IIb, CLK1
3mc syndrome, Carnevale syndrome, Coronary artery disease, Craniofacial abnormalities, Craniofacial ulnar renal syndrome, Desbuquois syndrome, Malpuech facial clefting syndrome, Metabolic syndrome, Oculopalatosekeletal syndrome, Diabetes mellitus, type 2

1014
Cell cycle regulator of NHEJ
C7orf49, CYREN-1, CYREN-2, MRI, MRI-2
Prostate cancer

1015
Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase
CDG1Z, DEE50, EIEE50, GATD4
Hypoplastic anemia, Sickle cell anemia, Beta thalassemia, Carbamoyl phosphate synthetase deficiency, Congenital esophageal anomaly, Congenital microcephaly, Aplastic anemia, Coronary artery disease, Developmental and epileptic encephalopathy, Epilepsy, Intellectual developmental disorder, Meniere disease, Spherocytosis

1016
CUE domain containing 2
C10orf66, bA18I14.5
Autism

1017
CaM kinase like vesicle associated
1G5, VACAMKL
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Inflammatory bowel disease, Osteoarthritis, Post-traumatic stress disorder

1018
Centromere protein M
C22orf18, CENP-M, PANE1
Hepatocellular carcinoma, Schizophrenia

1019
Coiled-coil domain containing 86
Cgr1
Diffuse large b-cell lymphoma, Schizophrenia

1020
Caspase recruitment domain family member 14
BIMP2, CARMA2, PRP, PSORS2, PSS1
Autoinflammatory syndrome, Central nervous system cancer, Glioblastoma, Glioma, Hirschsprung disease, Moyamoya disease, Mucopolysaccharidosis, Psoriasis, Psoriasis vulgaris, Seborrheic dermatitis, Skin disease