Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
861 to 870 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

861
CEA cell adhesion molecule 19
CEACM19, CEAL1
Alzheimer disease

862
CDC42 small effector 2
SPEC2
Alzheimer disease, Eczema, Crohn disease, Inflammatory bowel disease, Nasal polyp, Schizophrenia, Scoliosis, Ulcerative colitis

863
Choline phosphotransferase 1
CPT, CPT1
Orofacial cleft

864
Coenzyme Q8A
ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9
Autosomal recessive ataxia, Cerebellar ataxia, Cataract, Cerebellar atrophy, Coenzyme q10 deficiency, Congenital neurologic anomalies , Global developmental delay, Gout, Mitochondrial disease, Nystagmus, Spinocerebellar ataxia

865
Coiled-coil domain containing 47
GK001, MSTP041, THNS
Trichohepatoneurodevelopmental syndrome

866
Calcium binding protein 4
CRSD, CSNB2B
Nocturnal frontal lobe epilepsy, Cone dystrophy, Cone-rod dystrophy, Night blindness, congenital stationary, Ocular albinism, Optic atrophy, Retinitis pigmentosa, Usher syndrome

867
Coenzyme Q9
C16orf49, COQ10D5
Coenzyme q10 deficiency, Leigh syndrome, Mitochondrial disease

868
Cas scaffold protein family member 4
C20orf32, CAS4, HEFL, HEPL
Alzheimer disease, Dementia, Hypertension

869
Carboxypeptidase A6
CPAH, ETL5, FEB11
Alzheimer disease, Cerebral amyloid angiopathy, Cerebral palsy, Epilepsy, Familial temporal lobe epilepsy, Rolandic epilepsy, Febrile convulsion, Gastroesophageal reflux disease, Generalized epilepsy with febrile seizures plus, Global developmental delay, Intellectual developmental disorder, Oligodendroglioma, Periventricular heterotopia, Seizures, Tuberculosis
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870
Cysteinyl leukotriene receptor 2
CYSLT2, CYSLT2R, GPCR21, HG57, HPN321, KPG_011, PSEC0146, hGPCR21
Asthma, Atrial fibrillation, Ovarian epithelial cancer, Ovarian cancer, Pulmonary fibrosis, Juvenile idiopathic arthritis, Uveal melanoma