Genes | GeDiPNet - Gene Disease Pathway & Associations

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13091 to 13100 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
13091	8224	SYN3	Synapsin III	-	Cerebral arteriovenous malformations, Atrophic macular degeneration, Benign prostatic hyperplasia, Bipolar disorder, Brain aneurysm, Cerebellar vermis atrophy, Obstructive pulmonary disease, Coronary artery disease, Glaucoma, Global developmental delay, Insomnia, Major depressive disorder, Open angle glaucoma, Schizophrenia, Age-related macular degeneration
13092	81493	SYNC	Syncoilin, intermediate filament protein	SYNC1, SYNCOILIN	Diabetes mellitus type 2
13093	10492	SYNCRIP	Synaptotagmin binding cytoplasmic RNA interacting protein	GRY-RBP, GRYRBP, HNRNPQ, HNRPQ1, NSAP1, PP68, hnRNP-Q	Autism, Leukemia, Neurodevelopmental disorder, Non-specific syndromic intellectual disability
13094	79953	SYNDIG1	Synapse differentiation inducing 1	C20orf39, DSPC2, IFITMD5, TMEM90B	Bipolar disorder, Asthma, Tourette syndrome, Osteonecrosis of the femoral head, Major depressive disorder, Metabolic syndrome, Ovarian cancer, Ovarian serous carcinoma, Periodontal disease, Periodontitis, Schizophrenia, Depression, Diabetes mellitus type 2
13095	646658	SYNDIG1L	Synapse differentiation inducing 1 like	CAPUCIN, DSPC1, IFITMD4, SynDIG2, TMEM90A	Crohn disease, Kidney cancer, Metabolic syndrome, Niemann-pick disease, Open angle glaucoma, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm
13096	23345	SYNE1	Spectrin repeat containing nuclear envelope protein 1	8B, AMC3, AMCM, ARCA1, C6orf98, CPG2, EDMD4, KASH1, MYNE1, Nesp1, SCAR8, dJ45H2.2	Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Autism, Emery-dreifuss muscular dystrophy, Autosomal recessive ataxia, Cerebellar ataxia, Bipolar disorder, Breast neoplasms, Cardiomyopathy, Dilated cardiomyopathy, Colorectal neoplasms, Atrioventricular block, Coronary artery disease, Bipolar depression, Endometriosis View all (12 more)
13097	23224	SYNE2	Spectrin repeat containing nuclear envelope protein 2	EDMD5, KASH2, NUA, NUANCE, Nesp2, Nesprin-2, SYNE-2, TROPH	Anorexia nervosa, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Emery-dreifuss muscular dystrophy, Bipolar disorder, Renal cell carcinoma, Cardiac arrhythmia, Cardioembolic stroke, Dilated cardiomyopathy, Cerebral palsy, Melanoma, Left ventricular disease, Long qt syndrome View all (8 more)
13098	161176	SYNE3	Spectrin repeat containing nuclear envelope family member 3	C14orf139, C14orf49, KASH3, LINC00341, NCRNA00341, NET53, Nesp3	Atrial fibrillation, Obesity, Open angle glaucoma, Squamous cell carcinoma, Waldenstrom macroglobulinemia
13099	163183	SYNE4	Spectrin repeat containing nuclear envelope family member 4	C19orf46, DFNB76, KASH4, Nesp4	Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing loss, Nonsyndromic hearing loss
13100	8831	SYNGAP1	Synaptic Ras GTPase activating protein 1	MRD5, RASA1, RASA5, SYNGAP	Autism, Nonsyndromic intellectual disability, Blepharoptosis, Cerebellar ataxia, Neurodevelopmental disorder, Developmental disability, Epilepsy, Epilepsy with myoclonic atonic seizures, Developmental and epileptic encephalopathy, Global developmental delay, Inflammatory bowel disease, Insomnia, Intellectual developmental disorder, Alzheimer disease, Multiple sclerosis View all (5 more)

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