Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
391 to 400 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

391
SAC3 domain containing 1
HSU79266, SHD1
Melanoma

392
SEC61 translocon subunit alpha 1
ADTKD5, CVID15, HNFJ4, HSEC61, SEC61, SEC61A
Tubulointerstitial kidney disease, Common variable immunodeficiency, Craniofacial abnormalities, Hyperuricemic nephropathy, Neutropenia, Severe congenital neutropenia, Polycystic liver disease, Prostate cancer, Congenital neutropenia

393
SERTA domain containing 1
SEI1, TRIP-Br1, TRIPBR1
Colonic neoplasm, Mood disorder

394
Solute carrier family 25 member 24
APC1, SCAMC-1, SCAMC1
Crohn disease, Dementia, Dental caries, Desbuquois syndrome, Eosinophilia, Heart failure, Inflammatory bowel disease, Liver cirrhosis, Ulcerative colitis

395
Schwannomin interacting protein 1
SCHIP-1
B-cell acute lymphoblastic leukemia, Asthma, Color vision deficiency, Neurodevelopmental disorder, Congenital hemihypertrophy, Conotruncal cardiac defect, Non-specific syndromic intellectual disability, Biliary cholangitis, Scoliosis, Severe acute respiratory syndrome, Systemic lupus erythematosus

396
Solute carrier family 39 member 3
ZIP-3, ZIP3
Bipolar disorder, Non-organic psychosis, Psychotic disorders, Schizophrenia

397
SH3 domain containing kinase binding protein 1
AGMX2, CD2BP3, CIN85, GIG10, HSB-1, HSB1, IMD61, MIG18
Colonic neoplasm, Immunodeficiency, X-linked common variable immunodeficiency phenotype due to sh3kbp1 deficiency

398
Solute carrier family 40 member 1
FPN, FPN1, HFE4, IREG1, MST079, MSTP079, MTP1, SLC11A3
Anemia, Autism, Bone fracture, Ferroxidase deficiency, Endometriosis, Apoceruloplasmin deficiency, Hemochromatosis, Hemolysis, Hereditary hemochromatosis, Iron overload, Liver neoplasm, Open angle glaucoma, Osteoarthritis, Willis-ekbom disease

399
Serpin family D member 1
D22S673, HC2, HCF2, HCII, HLS2, LS2, THPH10
Carotid artery thrombosis, Heparin cofactor 2 deficiency, Venous thromboembolism

400
SRY-box transcription factor 8
-
Multiple sclerosis, Neurodevelopmental disorders, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy, Polycystic ovary syndrome