Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

151 to 160 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
151	10845	CLPX	Caseinolytic mitochondrial matrix peptidase chaperone subunit X	EPP2	Protoporphyria, erythropoietic
152	10850	CCL27	C-C motif chemokine ligand 27	ALP, CTACK, CTAK, ESKINE, ILC, PESKY, SCYA27	Dermatitis, Malignant mesothelioma, Rheumatoid arthritis
153	10858	CYP46A1	Cytochrome P450 family 46 subfamily A member 1	CP46, CYP46	Alzheimer disease, Senile dementia
154	10877	CFHR4	Complement factor H related 4	CFHL4, FHR-4, FHR4	Complement component deficiency, Eczema, Hemolytic uremic syndrome, Age-related macular degeneration
155	10878	CFHR3	Complement factor H related 3	CFHL3, DOWN16, FHR-3, FHR3, HLF4	Complement component deficiency, Dysphasia, Geographic atrophy, Glomerulonephritis, Hemolytic uremic syndrome, Hyperlipidemia, Hypertension, Impaired cognition, Age-related macular degeneration, Microangiopathic hemolytic anemia
156	10951	CBX1	Chromobox 1	CBX, HP1-BETA, HP1Hs-beta, HP1Hsbeta, Hp1beta, M31, MOD1, p25beta	Prostatic neoplasms, Prostate cancer
157	10978	CLP1	Cleavage factor polyribonucleotide kinase subunit 1	HEAB, hClp1	Acquired kyphoscoliosis, Cerebral cortical atrophy, Congenital kyphoscoliosis, Cryptorchidism, Developmental delay, Epileptic encephalopathy, Esotropia, High palate, Hypoplasia of corpus callosum, Mental retardation, Nystagmus, Optic atrophy, Pontoneocerebellar hypoplasia, Proptosis, Sensorimotor neuropathy, Strabismus View all (1 more)
158	10987	COPS5	COP9 signalosome subunit 5	CSN5, JAB1, MOV-34, SGN5	Joubert syndrome, Liver carcinoma, Stevens-johnson syndrome
159	1103	CHAT	Choline O-acetyltransferase	CHOACTASE, CMS1A, CMS1A2, CMS6	Acquired kyphoscoliosis, Angle closure glaucoma, Arthrogryposis multiplex congenita, Bulbar palsy, Clonic seizures, Developmental dysplasia of the hip, Congenital kyphoscoliosis, Myasthenic syndrome, Congenital pectus carinatum, Distal amyotrophy, Dysphagia, Esotropia, External ophthalmoplegia, Febrile seizures, Gastroesophageal reflux disease View all (17 more)
160	1105	CHD1	Chromodomain helicase DNA binding protein 1	CHD-1, PILBOS	Apraxia, Autism, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Developmental delay, Frontal bossing, Immunologic deficiency syndromes, Intellectual disability-autism-speech apraxia-craniofacial dysmorphism syndrome, Macrocephaly, Memory disorders, Age-related memory disorders, Mental retardation, Pilarowski-bjornsson syndrome View all (3 more)

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