Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

1001 to 1010 of 1203 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1001	79751	SLC25A22	Solute carrier family 25 member 22	DEE3, EIEE3, GC-1, GC1, NET44	Developmental and epileptic encephalopathy, Developmental delay, Myoclonic encephalopathy, Epilepsy of infancy with migrating focal seizures, Malignant migrating partial seizures of infancy
1002	79753	SNIP1	Smad nuclear interacting protein 1	NEDHCS, PML1, PMRED	Rolandic epilepsy, Neurodevelopmental disorder
1003	79783	SUGCT	Succinyl-CoA:glutarate-CoA transferase	C7orf10, DERP13, GA3, ORF19	Asthma, Color vision deficiency, Hemorrhoid, Language development disorders, Melanoma, Migraine, Moyamoya disease, Pancreatic cancer, Pancreatic neoplasm, Peripheral neuropathy, Post-operative myocardial infarction, Prostate cancer, Testicular carcinoma, Diabetes mellitus, type 2
1004	7979	SEM1	SEM1 26S proteasome subunit	C7orf76, DSS1, ECD, PSMD15, SHFD1, SHFM1, SHSF1, Shfdg1	Attention deficit hyperactivity disorder, Bone disease, Bone fracture, Squamous cell carcinoma, Central nervous system cancer, Diverticular disease, Frontotemporal dementia, Glioblastoma, Glioma, Alzheimer disease, Oligodendroglioma, Osteoporosis, Sarcoidosis
1005	79794	SPRING1	SREBF pathway regulator in golgi 1	C12orf49, LUR1, POST1, SPRING	Asthma, Neurotic disorder
1006	79801	SHCBP1	SHC binding and spindle associated 1	PAL	Liver cirrhosis, Sarcoma
1007	79811	SLTM	SAFB like transcription modulator	Met	Asperger syndrome, Bipolar disorder, Jeune thoracic dystrophy, Major depressive disorder, Schizophrenia
1008	7982	ST7	Suppression of tumorigenicity 7	ETS7q, FAM4A, FAM4A1, HELG, RAY1, SEN4, TSG7	Brain atrophy, Central nervous system cancer, Crohn disease, Developmental and epileptic encephalopathy, Endometriosis, Glioma, Global developmental delay, Inflammatory bowel disease, Migraine, Seizures, Ulcerative colitis
1009	79856	SNX22	Sorting nexin 22	-	Osteogenesis imperfecta
1010	79925	SPEF2	Sperm flagellar 2	CT122, KPL2, SPGF43	Asthma, Eczema, Atrophic macular degeneration, Autoimmune thyroid disease, Biliary cirrhosis, Rhinosinusitis, Ciliary dyskinesia, Duchenne muscular dystrophy, Hypothyroidism, Multiple sclerosis, Nasal polyp, Nasal disorder, Biliary cholangitis, Psoriasis, Schizophrenia View all (5 more)

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