Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "S"

281 to 290 of 1203 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
281	23315	SLC9A8	Solute carrier family 9 member A8	NHE-8, NHE8	Amyotrophic lateral sclerosis, Ankylosing spondylitis, Coronary artery disease, Crohn disease, Dementia, Multiple sclerosis, Psoriasis, Psoriasis vulgaris, Sclerosing cholangitis, Ulcerative colitis
282	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 (10 more)
283	23334	SZT2	SZT2 subunit of KICSTOR complex	C1orf84, DEE18, EIEE18, KIAA0467, KICS1, SZT2A, SZT2B	Alzheimer disease, Developmental and epileptic encephalopathy, Generalized epilepsy, Rolandic epilepsy, Global developmental delay, Hypertension, Intellectual developmental disorder, Obesity, Parkinson disease
284	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, Colorectal neoplasm, Atrioventricular block, Coronary artery disease, Bipolar depression, Endometriosis, Female infertility View all (11 more)
285	23347	SMCHD1	Structural maintenance of chromosomes flexible hinge domain containing 1	BAMS, FSHD2	Arhinia-choanal atresia-microphthalmia syndrome, Atrial fibrillation, Bosma arhinia microphthalmia syndrome, Chediak-higashi syndrome, Conotruncal cardiac defect, Crohn disease, Cryptorchidism, Facial nerve disorder, Facioscapulohumeral muscular dystrophy, Inflammatory bowel disease, Male infertility single gene azoospermia, Muscular dystrophy, Myopathy, Diabetes mellitus, type 2, Ulcerative colitis
286	23353	SUN1	Sad1 and UNC84 domain containing 1	UNC84A	Atrial fibrillation, Atrial flutter, Insomnia
287	23380	SRGAP2	SLIT-ROBO Rho GTPase activating protein 2	ARHGAP34, FNBP2, SRGAP2A, SRGAP3	Asthma, Obstructive pulmonary disease, Intellectual developmental disorder, Developmental and epileptic encephalopathy, Respiratory system disease, Systemic lupus erythematosus, Diabetes mellitus, type 2
288	23384	SPECC1L	Sperm antigen with calponin homology and coiled-coil domains 1 like	CYTSA, GBBB2, OBLFC1, TBHS, TBHS1	Opitz g/bbb syndrome, Commissural facial cleft, Coronary artery disease, Craniosynostosis, Desbuquois syndrome, Intellectual developmental disorder, Major depressive disorder, Kawasaki disease, Myocardial infarction, Diabetes mellitus, type 2
289	23387	SIK3	SIK family kinase 3	L19, QSK, SEMDK, SIK-3	Eczema, Atrial fibrillation, Autism, Breast cancer, Cancer, Color vision deficiency, Coronary artery disease, Diabetes mellitus, Digestive system disease, Diverticular disease, Hearing impairment, Nonsyndromic hearing loss, Heart failure, Hypothyroidism, Metabolic syndrome View all (5 more)
290	23410	SIRT3	Sirtuin 3	SIR2L3	Brain aneurysm, Squamous cell carcinoma, Coronary artery disease, Gestational diabetes, Hypothyroidism, Mouth neoplasm, Obesity, Uterine fibroid

«««...27 282930 31...»»»