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
12381 to 12390 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

12381
Schlafen family member 11
SLFN8/9
Moyamoya angiopathy

12382
Schlafen family member 12
SLFN3
Barrett esophagus

12383
Schlafen family member 12 like
-
Duchenne muscular dystrophy, Major depressive disorder

12384
Schlafen family member 14
BDPLT20
Thrombocytopenia with platelet secretion defect, Platelet-type bleeding disorder, Breast cancer, Prostate cancer, Thrombocytopenia

12385
Schlafen family member 5
-
Alzheimer disease

12386
SRA stem-loop interacting RNA binding protein
C14orf156, DC50, PD04872
Mitochondrial encephalomyopathy

12387
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

12388
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, Rheumatic fever, Schizophrenia, Scoliosis, Small cell lung carcinoma, Substance abuse, Diabetes mellitus type 2

12389
Slit guidance ligand 3
MEGF5, SLIL2, SLIT1, Slit-3, slit2
Eczema, Atrial fibrillation, Bipolar disorder, Color vision deficiency, Congenital diaphragmatic hernia, Dry eye syndrome, Inflammatory skin disease, Major depressive disorder, Multiple sclerosis, Pelvic organ prolapse, Psoriasis, Schizophrenia, Scoliosis, Stroke, Depression

12390
SLIT and NTRK like family member 1
LRRC12, TTM
Color vision deficiency, Tourette syndrome, Hyperopia, Pancreatic cancer, Peripheral neuropathy, Scoliosis, Squamous cell carcinoma, Hypertension, Trichotillomania