Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "S"

1111 to 1120 of 1203 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1111	8878	SQSTM1	Sequestosome 1	A170, DMRV, EBIAP, FTDALS3, NADGP, OSIL, PDB3, ZIP3, p60, p62, p62B	Alzheimer disease, Amyotrophic lateral sclerosis, Developmental coordination disorder, Distal myopathy, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Frontotemporal dementia with motor neuron disease, Diabetes mellitus, type 2, Macular degeneration, Motor skills disorder, Osteoarthritis, Osteosarcoma, Paget disease, Peptic ulcer disease, Spastic paraplegia, Welander distal myopathy
1112	8879	SGPL1	Sphingosine-1-phosphate lyase 1	NPHS14, RENI, S1PL, SPL	Eczema, Attention deficit hyperactivity disorder, Charcot-marie-tooth disease, Hepatitis b virus infection, Digestive system disease, Hepatitis b, Hyperopia, Multiple myeloma, Nephrotic syndrome, Obesity, Willis-ekbom disease, Scoliosis, Seborrheic dermatitis, Substance abuse, Diabetes mellitus, type 2, Uveal melanoma View all (1 more)
1113	8884	SLC5A6	Solute carrier family 5 member 6	COMNB, NERIB, SMVT, SMVTD, hSMVT	Genetic neurodegenerative disease, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus, type 2, Uterine fibroid
1114	8910	SGCE	Sarcoglycan epsilon	DYT11, ESG, epsilon-SG	Major depressive disorder, Dystonia, Dystonia musculorum deformans, Genetic torsion dystonia, Insomnia, Depression, Movement disorder, Myoclonic dystonia, Schizophrenia
1115	8935	SKAP2	Src kinase associated phosphoprotein 2	PRAP, RA70, SAPS, SCAP2, SKAP-HOM, SKAP55R	Androgenetic alopecia, Ankylosing spondylitis, Venous insufficiency, Crohn disease, Inflammatory bowel disease, Liver cirrhosis, Multiple sclerosis, Psoriasis, Sclerosing cholangitis, Small cell lung carcinoma, Systemic lupus erythematosus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Ulcerative colitis
1116	89866	SEC16B	SEC16 homolog B, endoplasmic reticulum export factor	LZTR2, PGPR-p117, RGPR, RGPR-p117, SEC16S	Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Polycystic liver disease, Body weight, Bone fragility with contractures, arterial rupture, and deafness, Breast cancer, Color vision deficiency, Gout, Metabolic syndrome, Obesity, Osteoarthritis, Osteoporosis-pseudoglioma syndrome, Schizoaffective disorder, Schizophrenia, Scoliosis View all (2 more)
1117	89874	SLC25A21	Solute carrier family 25 member 21	MTDPS18, ODC, ODC1	Barrett esophagus, Breast cancer, Colorectal cancer, Coronary artery disease, Esophageal adenocarcinoma, Estrogen-receptor negative breast cancer, Migraine, Mitochondrial dna depletion syndrome, Ovarian cancer, Prostate cancer
1118	8991	SELENBP1	Selenium binding protein 1	EHMTO, HEL-S-134P, LPSB, MTO, SBP56, SP56, hSBP	Colorectal neoplasm, Lung neoplasms, Major depressive disorder, Myocardial infarction, Ovarian neoplasm, Psychotic disorders, Schizophrenia, Stomach neoplasms, Diabetes mellitus, type 2
1119	9021	SOCS3	Suppressor of cytokine signaling 3	ATOD4, CIS3, Cish3, SOCS-3, SSI-3, SSI3	Asthma, Atherosclerosis, Eczema, Hepatocellular carcinoma, Endometrial neoplasm, Inflammatory skin disease, Liver disease, Myocardial ischemia, Obesity, Osteoarthritis, Psoriasis, Respiratory system disease
1120	9037	SEMA5A	Semaphorin 5A	SEMAF, semF	Anophthalmia, Autism, Central nervous system cancer, Charcot-marie-tooth disease, Coronary artery disease, Dementia, Glioblastoma, Glioma, Infective arthritis, Intellectual developmental disorder, Myasthenia gravis, Neurodevelopmental disorders, Obesity, Parkinson disease, Hypogonadism View all (3 more)

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