Genes | GeDiPNet - Gene Disease Pathway & Associations

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11561 to 11570 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11561	6301	SARS1	Seryl-tRNA synthetase 1	NEDMAS, SARS, SERRS, SERS	Cerebral arteriovenous malformations, Nonsyndromic intellectual disability, Primary microcephaly, Ischemic heart disease, Coronary artery disease, Intellectual developmental disorder, Myocardial ischemia, Neurodevelopmental disorder
11562	54938	SARS2	Seryl-tRNA synthetase 2, mitochondrial	SARS, SARSM, SERS, SYS, SerRS, SerRSmt, mtSerRS	Hyperuricemia syndrome, Mitochondrial disease, Diabetes mellitus type 2
11563	9092	SART1	Spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP	Ara1, HAF, HOMS1, SART1259, SNRNP110, Snu66	Gout, Non-melanoma skin carcinoma, Osteoarthritis
11564	9733	SART3	Spliceosome associated factor 3, U4/U6 recycling protein	DSAP1, P100, RP11-13G14, TIP110, p110, p110(nrb)	Neurodevelopmental disorder, Disseminated superficial actinic porokeratosis, Non-specific syndromic intellectual disability, Open angle glaucoma, Porokeratosis
11565	23328	SASH1	SAM and SH3 domain containing 1	CAPOK, DUH, DUH1, SH3D6A, dJ323M4.1	Alzheimer disease, Autoimmune disease, Autoimmune thyroid disease, Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma, Colorectal cancer, Diabetic neuropathy, Dilated cardiomyopathy, Dyschromatosis, Dyschromatosis symmetrica hereditaria, Esophageal cancer, Esophageal disease, Esophageal ulcer, Gastric cancer, Glioma, Hepatolenticular degeneration View all (9 more)
11566	54440	SASH3	SAM and SH3 domain containing 3	753P9, CXorf9, HACS2, IMD102, SH3D6C, SLY	Combined immunodeficiency, x-linked, Immunodeficiency, Liver cirrhosis, X-linked combined immunodeficiency diseases
11567	163786	SASS6	SAS-6 centriolar assembly protein	MCPH14, SAS-6, SAS6	Primary microcephaly, Microcephaly
11568	6303	SAT1	Spermidine/spermine N1-acetyltransferase 1	DC21, KFSD, KFSDX, SAT, SSAT, SSAT-1	Anxiety disorder, Bipolar disorder, Major depressive disorder, Allergic contact dermatitis, Keratosis follicularis spinulosa decalvans, Mood disorder, Non-organic psychosis, Obesity, Psychotic disorders, Schizoaffective disorder, Systemic lupus erythematosus, Depression
11569	6304	SATB1	SATB homeobox 1	DEFDA, DHDBV, KTZSL	Eczema, Autism, Breast cancer, Neurodevelopmental disorder, Den hoed-de boer-voisin syndrome, Developmental delay with dysmorphic facies and dental anomalies, Duchenne muscular dystrophy, Hyperaldosteronism, Intellectual developmental disorder seizures extrapyramidal, Lung cancer, Non-specific syndromic intellectual disability, Venous thromboembolism
11570	23314	SATB2	SATB homeobox 2	C2DELq32q33, DEL2Q32Q33, GLSS	Autism, Cancer, Cerebellar ataxia, Chromosome 2q32-q33 deletion syndrome, Cleft palate, Clinodactyly, Colorectal cancer, Colorectal neoplasms, Craniofacial abnormalities, Desbuquois syndrome, Developmental disability, Dyslexia, Gastroesophageal reflux disease, Glass syndrome, Global developmental delay View all (10 more)

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