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
12321 to 12330 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

12321
Solute carrier organic anion transporter family member 6A1
CT48, GST, OATP-I, OATP6A1, OATPY
Color vision deficiency, Diabetes mellitus, Metabolic syndrome, Orofacial cleft, Schizophrenia, Diabetes mellitus type 2

12322
SMC5/6 complex localization factor 2
ATELS1, C10orf6, FAM178A, hNSE6
Atelis syndrome, Lung cancer, Mosaic variegated aneuploidy, Nonalcoholic fatty liver disease, Squamous cell carcinoma, Diabetes mellitus type 2

12323
Schlafen family member 11
SLFN8/9
Moyamoya angiopathy

12324
Schlafen family member 12
SLFN3
Barrett esophagus

12325
Schlafen family member 12 like
-
Duchenne muscular dystrophy, Major depressive disorder

12326
Schlafen family member 14
BDPLT20
Thrombocytopenia with platelet secretion defect, Platelet-type bleeding disorder, Breast cancer, Prostate cancer, Thrombocytopenia

12327
Schlafen family member 5
-
Alzheimer disease

12328
SRA stem-loop interacting RNA binding protein
C14orf156, DC50, PD04872
Mitochondrial encephalomyopathy

12329
Slit guidance ligand 1
MEGF4, SLIL1, SLIT-1, SLIT3
Monomelic amyotrophy, Arthritis, Attention deficit hyperactivity disorder, Bipolar disorder, Central nervous system cancer, Glioblastoma, Glioma, Obesity, Ulcerative colitis

12330
Slit guidance ligand 2
SLIL3, Slit-2
Attention deficit hyperactivity disorder, Congenital anomalies of the kidney and urinary tract, Hepatocellular carcinoma, Congenital anomalies of kidney and urinary tract, Temporal lobe epilepsy, Promyelocytic leukemia, Metabolic syndrome, Schizophrenia, Scoliosis, Small cell lung carcinoma, Substance abuse, Diabetes mellitus type 2