Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

861 to 870 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
861	56971	CEACAM19	CEA cell adhesion molecule 19	CEACM19, CEAL1	Alzheimer disease
862	56990	CDC42SE2	CDC42 small effector 2	SPEC2	Alzheimer disease, Crohn disease, Inflammatory bowel disease, Schizophrenia
863	56994	CHPT1	Choline phosphotransferase 1	CPT, CPT1	Respiratory distress syndrome
864	56997	COQ8A	Coenzyme Q8A	ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9	Anxiety disorder, Ataxia, Cerebellar ataxia, Cerebellar atrophy, Coenzyme q10 deficiency, Developmental regression, Gynecomastia, Mental retardation, Mitochondrial diseases, Nystagmus, Spinocerebellar ataxia, Strabismus
865	57003	CCDC47	Coiled-coil domain containing 47	GK001, MSTP041, THNS	Brachycephaly, Central visual impairment, Cerebral atrophy, Congenital clubfoot, Developmental delay, Distal arthrogryposis, Gastroesophageal reflux disease, High palate, Hyperopia, Hypoplasia of nipple, Macroglossia, Mental retardation, Microcephaly, Microdontia, Otitis media View all (5 more)
866	57010	CABP4	Calcium binding protein 4	CRSD, CSNB2B	Achromatopsia, Cone dystrophy, Cone-rod dystrophy, Congenital stationary night blindness, Disorder of eye, Hypoplasia of optic disc, Myopia, Night blindness, Nocturnal epilepsy, Nyctalopia, Nystagmus, Retinal dystrophy, Strabismus
867	57017	COQ9	Coenzyme Q9	C16orf49, COQ10D5	Cerebellar atrophy, Cerebral atrophy, Coenzyme q10 deficiency, Developmental delay, Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome, Epileptic encephalopathy, Hyperglycemia, Left ventricular hypertrophy
868	57091	CASS4	Cas scaffold protein family member 4	C20orf32, CAS4, HEFL, HEPL	Alzheimer disease, Senile dementia
869	57094	CPA6	Carboxypeptidase A6	CPAH, ETL5, FEB11	Benign mesial temporal lobe epilepsy, Epilepsy, Febrile seizures, Mesial temporal lobe epilepsy with febrile seizures, Periventricular gray matter heterotopia, Seizure
870	57105	CYSLTR2	Cysteinyl leukotriene receptor 2	CYSLT2, CYSLT2R, GPCR21, HG57, HPN321, KPG_011, PSEC0146, hGPCR21	Alveolitis, Asthma, Cataract, Choroidal melanoma, Congenital cataract, Inferior lens subluxation, Inflammatory abnormality of the eye, Iris melanoma, Ciliary body melanoma, Ocular hypertension, Pulmonary fibrosis, Retinal detachment, Uveal melanoma

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