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
11531 to 11540 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11531
S-antigen visual arrestin
RP47, RP96, S-AG
Cone dystrophy, Crohn disease, Inflammatory bowel disease, Nephrolithiasis, Night blindness, congenital stationary, Oguchi disease, Pancreatic cancer, Retinitis pigmentosa, Diabetes mellitus type 2, Uveitis

11532
Spalt like transcription factor 1
HEL-S-89, HSAL1, Sal-1, TBS, ZNF794
Alzheimer disease, Congenital anomalies of the kidney and urinary tract, Congenital abnormalities, Dental caries, Desbuquois syndrome, Diabetes mellitus, Gastroesophageal reflux disease, Insomnia, Congenital anomaly of limb, Middle lobe syndrome, Post-traumatic stress disorder, Scoliosis, Townes-brocks syndrome, Vacterl association

11533
Spalt like transcription factor 2
COLB, HSAL2, Sal-2, ZNF795, p150(Sal2)
Cleft eyelid, Coloboma, Commissural facial cleft, Congenital iris coloboma, Congenital ocular coloboma

11534
Spalt like transcription factor 3
ZNF796
Burkitt lymphoma, Craniofacial abnormalities, Gastrointestinal stromal tumor, Metabolic syndrome, Prostate cancer, Diabetes mellitus type 2

11535
Spalt like transcription factor 4
DRRS, HSAL4, IVIC, ZNF797
Craniofacial abnormalities, Desbuquois syndrome, Duane retraction syndrome, Duane-radial ray syndrome, Esophageal squamous cell carcinoma, Congenital heart septal defect, Congenital anomaly of limb, Neuroblastoma, Oculopalatosekeletal syndrome, Severe combined immunodeficiency, Ventricular septal defect

11536
Sterile alpha motif domain containing 11
MRS
Liver cirrhosis, Optic atrophy, Retinitis pigmentosa

11537
Sterile alpha motif domain containing 12
BAFME, BAFME1, FAME, FAME1, FCMTE1, MEBA
Benign myoclonic epilepsy, Bone fracture, Myoclonic epilepsy, Familial adult myoclonic epilepsy, Benign adult familial myoclonic epilepsy, Adult myoclonic epilepsy, Multiple sclerosis

11538
Sterile alpha motif domain containing 13
DJL, HSD-41, HSD-42
Metabolic syndrome, Neurotic disorder, Obesity, Diabetes mellitus type 2

11539
Sterile alpha motif domain containing 15
C14orf174, FAM15A
Diabetes mellitus type 2

11540
Sterile alpha motif domain containing 3
-
Major depressive disorder, Male reproductive organ cancer, Oligodendroglioma, Schizophrenia