Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11951 to 11960 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11951
Shisa like 2A
FAM159A, PRO7171, WWLS2783
Atrial fibrillation, Dementia

11952
SH3KBP1 binding protein 1
PP203, Sb1
Duchenne muscular dystrophy, Schizophrenia

11953
Shieldin complex subunit 1
C20orf196, RINN3
Breast cancer, Glomerulonephritis

11954
Shieldin complex subunit 2
FAM35A, FAM35A1, RINN2, bA163M19.1
Gout, Hyperinsulinemic hypoglycemia, Hyperinsulinism, Nephrolithiasis

11955
Serine hydroxymethyltransferase 1
CSHMT, SHMT
Breast neoplasms, Hodgkin lymphoma, Nervous system disease, Schizophrenia, Uterine fibroid

11956
Serine hydroxymethyltransferase 2
GLYA, HEL-S-51e, NEDCASB, SHMT, mSHMT
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Non-small-cell lung carcinoma, Neurodevelopmental disorder, Gout, Major depressive disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

11957
Shortage in chiasmata 1
C9orf84, MZIP2, SPGF75, ZIP2, ZIP2H
Coronary artery disease, Lung cancer, Male infertility, Male infertility single gene azoospermia, Spermatogenic failure, Testicular azoospermia

11958
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

11959
SHOX homeobox
GCFX, PHOG, SHOX1, SHOXY, SS
Connective tissue disease, Desbuquois syndrome

11960
SHOX homeobox 2
OG12, OG12X, SHOT
Atrial fibrillation, Basal cell carcinoma, Lung cancer, Major depressive disorder, Schizophrenia