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"
891 to 900 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

891
SLIT and NTRK like family member 5
LRRC11, bA364G4.2
Autism, Obsessive-compulsive disorder

892
SLIT and NTRK like family member 6
DFNMYP
Isolated sensorineural deafness, Color vision deficiency, Colorectal cancer, Deafness and myopia, Deafness, Dementia, Gestational diabetes, Global developmental delay, Hearing impairment, Hearing loss, Lewy body disease, Marshall syndrome, Metabolic syndrome, Oligodendroglioma, Scoliosis
View all (1 more)

893
STE20 like kinase
LOSK, STK2, bA16H23.1, se20-9
Atrial fibrillation, Basal cell carcinoma, Benign prostatic hyperplasia, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Clear cell renal cell carcinoma, Colorectal cancer, Coronary artery disease, Melanoma, Diabetic retinopathy, Differentiated thyroid carcinoma, Endometrial cancer, Esophageal cancer
View all (17 more)

894
Sarcolemma associated protein
SLAP
Alzheimer disease, Brugada syndrome, Cardiac arrest, Obstructive pulmonary disease, Long qt syndrome, Obesity, Diabetes mellitus type 2

895
Sarcolipin
-
Central nervous system cancer, Glioblastoma, Glioma

896
Secretory leukocyte peptidase inhibitor
ALK1, ALP, BLPI, HUSI, HUSI-I, MPI, WAP4, WFDC4
Asthma

897
SAFB like transcription modulator
Met
Asperger syndrome, Bipolar disorder, Jeune thoracic dystrophy, Major depressive disorder, Schizophrenia

898
Secreted LY6/PLAUR domain containing 1
ANUP, ARS, ArsB, LY6-MT, LY6LS, MDM
Mal de meleda, Meleda disease

899
SLX4 structure-specific endonuclease subunit
BTBD12, FANCP, MUS312
Fanconi anemia, Hereditary breast cancer, Metabolic syndrome, Pituitary stalk interruption syndrome, Diabetes mellitus type 2

900
SLX4 interacting protein
C20orf94, bA204H22.1, bA254M13.1, dJ1099D15.3
Androgenetic alopecia, Prostate cancer