Genes | GeDiPNet - Gene Disease Pathway & Associations

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2731 to 2740 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2731	1268	CNR1	Cannabinoid receptor 1	CANN6, CB-R, CB1, CB1A, CB1K5, CB1R, CNR	Anxiety disorder, Attention deficit hyperactivity disorder, Binge eating disorder, Bipolar disorder, Cannabis abuse, Catalepsy, Cholelithiasis, Cognition disorder, Conduct disorder, Delirium, dementia, and cognitive disorders, Major depressive disorder, Developmental coordination disorder, Diabetes mellitus type 2, Endometrial neoplasms, Endometriosis View all (24 more)
2732	1269	CNR2	Cannabinoid receptor 2	CB-2, CB2, CX5	Anterior cruciate ligament injury, Atherosclerosis, Bipolar disorder, Breast neoplasms, Cannabis abuse, Catalepsy, Cholelithiasis, Major depressive disorder, Immune system disorder, Endometrial neoplasms, Hyperalgesia, Hyperemia, Hyperglycemia, Immune system disease, Inflammatory bowel disease View all (9 more)
2733	25927	CNRIP1	Cannabinoid receptor interacting protein 1	C2orf32, CRIP-1, CRIP1	Deafness
2734	163882	CNST	Consortin, connexin sorting protein	C1orf71, PPP1R64	Osteoarthritis, Thyroid disease
2735	124817	CNTD1	Cyclin N-terminal domain containing 1	CNTD, COSA1	Breast cancer
2736	1270	CNTF	Ciliary neurotrophic factor	HCNTF	Amyotrophic lateral sclerosis, Cerebral hemorrhage, Major depressive disorder, Glaucoma, Huntington disease, Motor neuron disease, Multiple sclerosis, Obesity, Schizophrenia
2737	1271	CNTFR	Ciliary neurotrophic factor receptor	-	Osteoarthritis, Scoliosis
2738	54875	CNTLN	Centlein	C9orf101, C9orf39, bA340N12.1	Anorexia nervosa, Attention deficit hyperactivity disorder, Hemolytic anemia, Insomnia, Lung cancer, Major depressive disorder, Oligodendroglioma, Scoliosis
2739	1272	CNTN1	Contactin 1	CMYO12, CMYP12, F3, GP135, MYPCN	Alzheimer disease, Astrocytoma, Bipolar disorder, Central nervous system cancer, Compton-north congenital myopathy, Congenital lethal myopathy , Congenital myopathy, Dementia, Dry eye syndrome, Glioma, Major depressive disorder, Parkinson disease, Schizophrenia, Spondylosis
2740	6900	CNTN2	Contactin 2	AXT, EPEO5, FAME5, TAG-1, TAX, TAX1	Benign myoclonic epilepsy, Neurodevelopmental disorder, Diabetes mellitus, Early onset epilepsy with developmental delay, Familial adult myoclonic epilepsy, Adult myoclonic epilepsy, Gout, Non-specific syndromic intellectual disability, Periodontitis, Schizophrenia, Diabetes mellitus type 2

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