Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "S"
881 to 890 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

881
Schlafen family member 14
BDPLT20
Thrombocytopenia with platelet secretion defect, Platelet-type bleeding disorder, Breast cancer, Prostate cancer, Thrombocytopenia

882
Schlafen family member 5
-
Alzheimer disease

883
SRA stem-loop interacting RNA binding protein
C14orf156, DC50, PD04872
Mitochondrial encephalomyopathy

884
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

885
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

886
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

887
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

888
SLIT and NTRK like family member 2
CXorf1, CXorf2, SLITL1, TMEM257, XLID111
Dyslexia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder

889
SLIT and NTRK like family member 3
-
Neurodevelopmental disorder, Epilepsy, Intellectual developmental disorder, Non-specific syndromic intellectual disability

890
SLIT and NTRK like family member 4
-
Uterine fibroid