Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
451 to 460 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

451
SHOC2 leucine rich repeat scaffold protein
NSLH1, SIAA0862, SOC2, SUR8
Anxiety disorder, Cardiofaciocutaneous syndrome, Cardiomyopathy, Costello syndrome, Atopic dermatitis, Desbuquois syndrome, Non-immune hydrops fetalis, Metabolic syndrome, Noonan syndrome, Polycystic kidney disease, Diabetes mellitus type 2

452
SHOX homeobox
GCFX, PHOG, SHOX1, SHOXY, SS
Connective tissue disease, Desbuquois syndrome

453
SHOX homeobox 2
OG12, OG12X, SHOT
Atrial fibrillation, Basal cell carcinoma, Lung cancer, Major depressive disorder, Schizophrenia

454
Sedoheptulokinase
CARKL, SHK
Sedoheptulokinase deficiency, Dementia

455
SNF2 histone linker PHD RING helicase
RAD5, bA545I5.2
Gastric cancer

456
SHQ1, H/ACA ribonucleoprotein assembly factor
DYT35, GRIM-1, NEDDS, Shq1p
Diabetes mellitus, Dystonia, Torsion dystonia, Early-onset generalized limb-onset dystonia, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2

457
Shroom family member 1
APXL2
Metabolic syndrome, Diabetes mellitus type 2

458
Shroom family member 2
APXL, HSAPXL
Colorectal cancer, Meniere disease, Prostate cancer

459
Shroom family member 3
APXL3, MSTP013, SHRM, ShrmL
Alzheimer disease, Atrial fibrillation, Cholecystolithiasis, Kidney disease, Coronary artery disease, Craniofacial microsomia, Eosinophilia, Gallstones, Intrahepatic cholestasis of pregnancy, Metabolic syndrome, Myocardial infarction, Nephrolithiasis, Neural tube defect, Parkinson disease, Prostate cancer
View all (4 more)

460
Shroom family member 4
MRXSSDS, SHAP, shrm4
Neurodevelopmental disorder, Congenital anomalies of kidney and urinary tract, Epilepsy, Insomnia, Intellectual developmental disorder, Non-specific syndromic intellectual disability, X-linked complex neurodevelopmental disorder, X-linked intellectual disability