Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
611 to 620 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

611
STAM binding protein like 1
ALMalpha, AMSH-FP, AMSH-LP, bA399O19.2
Aortic aneurysm, Connective tissue disease, Lung cancer, Lung carcinoma, Moyamoya disease, Multisystemic smooth muscle dysfunction syndrome, Nasopharyngeal carcinoma, Thoracic aortic aneurysm, Thoracic aortic aneurysm and aortic dissection

612
Signal induced proliferation associated 1 like 2
SPAL2, SPAR2
Charcot-marie-tooth disease, Parkinson disease, Schizophrenia

613
SLAIN motif family member 2
KIAA1458
Crohn disease, Inflammatory bowel disease, Uterine fibroids, Plexiform leiomyoma

614
Shroom family member 3
APXL3, MSTP013, SHRM, ShrmL
Coronary artery disease, Diabetes, Diabetes mellitus, Eosinophilia, Goldenhar syndrome, Kidney disease, Kidney failure, Leukemia, Neural tube defect, Situs ambiguus

615
Stromal interaction molecule 2
-
Leukemia

616
SH3 domain containing ring finger 1
POSH, RNF142, SH3MD2
Alzheimer disease

617
Shootin 1
KIAA1598, shootin-1
Oral cleft

618
Solute carrier family 7 member 14
PPP1R142
Cataract, Congenital hypoplasia of penis, Diabetes mellitus, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophy

619
Scm like with four mbt domains 2
-
Oestrogen receptor positive breast cancer

620
Spectrin beta, non-erythrocytic 4
CMND, NEDHND, QV, SPNB4, SPTBN3
Amyotrophy, Central visual impairment, Chromophobe carcinoma, Demyelinating neuropathy, Developmental delay, Distal amyotrophy, Facial paralysis, High palate, Neurodevelopmental disorder with hypotonia, neuropathy, and deafness, Sclerocystic ovaries, Papillary renal carcinoma, Polycystic ovary syndrome, Renal carcinoma, Scoliosis