Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

191 to 200 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
191	113189	CHST14	Carbohydrate sulfotransferase 14	ATCS, D4ST1, EDSMC1, HNK1ST	Alzheimer disease, Autism, Congenital clubfoot, Craniofacial abnormalities, Desbuquois syndrome, Ehlers-danlos syndrome, Gastric cancer, Prostatic neoplasm
192	1132	CHRM4	Cholinergic receptor muscarinic 4	HM4, M4R	Catatonia, Migraine, Schizophrenia, Tremor
193	113246	C12orf57	Chromosome 12 open reading frame 57	C10, GRCC10	Atrophy, Attention deficit hyperactivity disorder, Global developmental delay, Hydronephrosis, Intellectual developmental disorder, Microphthalmia, Vesicoureteral reflux
194	1133	CHRM5	Cholinergic receptor muscarinic 5	HM5	Internet addiction disorder, Schizophrenia, Substance abuse
195	11330	CTRC	Chymotrypsin C	CLCR, ELA4	Hereditary chronic pancreatitis, Pancreatitis
196	1134	CHRNA1	Cholinergic receptor nicotinic alpha 1 subunit	ACHRA, ACHRD, CHRNA, CMS1A, CMS1B, CMS2A, FCCMS, SCCMS	Autism, Centronuclear myopathy, Congenital myasthenic syndrome, Congenital myopathy, Epilepsy, Hydrops fetalis, Non-immune hydrops fetalis, Immune system disease, Myoclonic epilepsy, Myasthenia gravis, Myasthenic syndrome, Postsynaptic congenital myasthenic syndrome
197	1135	CHRNA2	Cholinergic receptor nicotinic alpha 2 subunit	-	Alzheimer disease, Nocturnal frontal lobe epilepsy, Bipolar disorder, Major depressive disorder, Gastroesophageal reflux disease, Intellectual developmental disorder, Lung cancer, Lung neoplasms, Depression, Myoclonic epilepsy, Schizophrenia, Seizures, Squamous cell carcinoma
198	1136	CHRNA3	Cholinergic receptor nicotinic alpha 3 subunit	BAIPRCK, LNCR2, NACHRA3, PAOD2	Amyotrophic lateral sclerosis, Anorexia nervosa, Aortic aneurysm, Atherosclerosis, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bladder dysfunction, Chronic bronchitis, Lung disease, Obstructive airway disease, Obstructive pulmonary disease, Dental caries, Lung cancer, Lung neoplasms View all (11 more)
199	113612	CYP2U1	Cytochrome P450 family 2 subfamily U member 1	P450TEC, SPG49, SPG56	Autism, Spastic paraplegia, Congenital neurologic anomalies�, Global developmental delay, Intellectual developmental disorder, Hereditary spastic paraplegia
200	1137	CHRNA4	Cholinergic receptor nicotinic alpha 4 subunit	BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4	Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism, Nocturnal frontal lobe epilepsy, Bronchus cancer, Lung disease, Obstructive pulmonary disease, Color vision deficiency, Depression, Major depressive disorder, Developmental and epileptic encephalopathy, Developmental disability, Dystonia, Frontal lobe epilepsy, Frontotemporal dementia View all (7 more)

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