Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1001 to 1010 of 1796 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1001	55584	CHRNA9	Cholinergic receptor nicotinic alpha 9 subunit	HSA243342, NACHRA9	Dementia
1002	1140	CHRNB1	Cholinergic receptor nicotinic beta 1 subunit	ACHRB, CHRNB, CMS1D, CMS2A, CMS2C, SCCMS	Breast cancer, Congenital myasthenic syndrome, Corneal dystrophy, Diverticular disease, Eye disease, Myasthenic syndrome, Parkinson disease, Postsynaptic congenital myasthenic syndrome, Diabetes mellitus type 2
1003	1141	CHRNB2	Cholinergic receptor nicotinic beta 2 subunit	EFNL3, nAChRB2	Alzheimer disease, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Nocturnal frontal lobe epilepsy, Colorectal cancer, Frontal lobe epilepsy, Focal onset epileptic seizure, Seizure, Neutropenia, Schizophrenia, Substance abuse
1004	1142	CHRNB3	Cholinergic receptor nicotinic beta 3 subunit	-	Attention deficit hyperactivity disorder, Bipolar disorder, Bipolar depression, Major depressive disorder, Parkinson disease, Substance abuse
1005	1143	CHRNB4	Cholinergic receptor nicotinic beta 4 subunit	-	Amyotrophic lateral sclerosis, Aneurysm, Aortic stenosis, Aortic valve disease, Obstructive airway disease, Obstructive pulmonary disease, Coronary artery disease, Dental caries, Frontotemporal dementia, Hypertrophic cardiomyopathy, Large artery stroke, Lung cancer, Lung neoplasms, Obesity, Obsessive-compulsive disorder View all (8 more)
1006	1144	CHRND	Cholinergic receptor nicotinic delta subunit	ACHRD, CMS2A, CMS3A, CMS3B, CMS3C, FCCMS, SCCMS	Arthrogryposis multiplex congenita, Blepharoptosis, Centronuclear myopathy, Congenital myasthenic syndrome, Myasthenic syndrome, Paralysis, Pena-shokeir syndrome , Postsynaptic congenital myasthenic syndrome
1007	1145	CHRNE	Cholinergic receptor nicotinic epsilon subunit	ACHRE, CMS1A1, CMS1D, CMS1E, CMS2A, CMS4A, CMS4B, CMS4C, FCCMS, FIM1, FIMG, FIMG1, MGI, SCCMS	Alzheimer disease, Blepharoptosis, Congenital myasthenic syndrome, Myasthenic syndrome, Postsynaptic congenital myasthenic syndrome, Diabetes mellitus type 2
1008	1146	CHRNG	Cholinergic receptor nicotinic gamma subunit	ACHRG	Arthrogryposis, Arthrogryposis multiplex congenita, Bone disease, Hypo-akinesia disorder of prenatal onset, Myasthenia gravis, Myasthenic syndrome, Pena-shokeir syndrome , Peripheral neuropathy, Rheumatoid arthritis, Scoliosis
1009	8534	CHST1	Carbohydrate sulfotransferase 1	C6ST, GST-1, KS6ST, KSGal6ST, KSST	Alzheimer disease, Autism, Gout, Hypertrophic cardiomyopathy, Insomnia, Obesity, Pelvic organ prolapse, Prostate cancer, Hypertension, Diabetes mellitus type 2
1010	9486	CHST10	Carbohydrate sulfotransferase 10	HNK-1ST, HNK1ST	Alzheimer disease, Autism

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