Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

1591 to 1600 of 1631 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1591	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
1592	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
1593	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 neoplasm, Cardiomyopathy, Dilated cardiomyopathy, Colorectal neoplasm, Atrioventricular block, Coronary artery disease, Bipolar depression, Endometriosis View all (12 more)
1594	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)
1595	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
1596	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
1597	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)
1598	9145	SYNGR1	Synaptogyrin 1	-	Biliary cirrhosis, Bipolar disorder, Crohn disease, Hypothyroidism, Inflammatory bowel disease, Myeloid leukemia, Systemic lupus erythematosus, Ovarian cancer, Biliary cholangitis, Rheumatoid arthritis, Schizophrenia, Ulcerative colitis
1599	9144	SYNGR2	Synaptogyrin 2	-	Lung cancer, Squamous cell carcinoma, Vitiligo
1600	8867	SYNJ1	Synaptojanin 1	DEE53, EIEE53, INPP5G, PARK20	Alzheimer disease, Juvenile parkinsonism, Basal cell carcinoma, Developmental and epileptic encephalopathy, Parkinson disease

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