Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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
11901 to 11910 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11901
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

11902
SHOX homeobox
GCFX, PHOG, SHOX1, SHOXY, SS
Connective tissue disease, Desbuquois syndrome

11903
SHOX homeobox 2
OG12, OG12X, SHOT
Atrial fibrillation, Basal cell carcinoma, Lung cancer, Major depressive disorder, Schizophrenia

11904
Sedoheptulokinase
CARKL, SHK
Sedoheptulokinase deficiency, Dementia

11905
SNF2 histone linker PHD RING helicase
RAD5, bA545I5.2
Gastric cancer

11906
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

11907
Shroom family member 1
APXL2
Metabolic syndrome, Diabetes mellitus type 2

11908
Shroom family member 2
APXL, HSAPXL
Colorectal cancer, Meniere disease, Prostate cancer

11909
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)

11910
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