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"
481 to 490 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
Salt inducible kinase 1
DEE30, MSK, SIK, SIK-1, SIK1B, SNF1LK
Alzheimer disease, Juvenile arthritis, Asthma, Dilated cardiomyopathy, Developmental and epileptic encephalopathy, Myoclonic encephalopathy, Generalized epilepsy, Global developmental delay, Hypertension, Juvenile idiopathic arthritis, Language development disorders, Oligoarticular juvenile idiopathic arthritis, West syndrome

482
Salt inducible kinase 2
LOH11CR1I, QIK, SIK-2, SNF1LK2
Asthma, Eczema, Breast cancer, Hepatocellular carcinoma, Coronary artery disease, Hypertension, Prostate cancer, Respiratory system disease, Sclerosing cholangitis

483
SIK family kinase 3
L19, QSK, SEMDK, SIK-3
Eczema, Atrial fibrillation, Autism, Breast cancer, Cancer, Color vision deficiency, Coronary artery disease, Diabetes mellitus, Digestive system disease, Diverticular disease, Hearing impairment, Hearing loss, Heart failure, Hypothyroidism, Metabolic syndrome
View all (5 more)

484
Suppressor of IKBKE 1
SIKE
Schizophrenia

485
SIL1 nucleotide exchange factor
BAP, MSS, ULG5
Alzheimer disease, Apraxia, Atrial fibrillation, Blepharoptosis, Cataract, Cerebellar atrophy, Global developmental delay, Insomnia, Marinesco-sjogren syndrome, Prostatic neoplasms, Strabismus

486
SIM bHLH transcription factor 1
bHLHe14
Androgenetic alopecia, Atrial fibrillation, Bipolar disorder, Breast neoplasms, Venous insufficiency, Neurodevelopmental disorder, Erectile dysfunction, Heart failure, Hyperglycemia, Insomnia, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Neurotic disorder, Non-specific syndromic intellectual disability
View all (4 more)

487
SIM bHLH transcription factor 2
HMC13F06, HMC29C01, SIM, bHLHe15
Asthma, Cleft palate, Craniofacial abnormalities, Prostate cancer, Seasonal allergic rhinitis, Testicular carcinoma

488
SIN3 transcription regulator family member A
CHR15DELq24, DEL15Q24, WITKOS
15q24 microdeletion, 15q24 microdeletion syndrome, Autism, Breast cancer, Chromosome 15q24 deletion syndrome, Congenital diaphragmatic hernia, Craniofacial abnormalities, Dwarfism, Gout, Hydrocephalus, Intellectual developmental disorder, Microcephaly, Neurodevelopmental disorder, Diabetes mellitus type 2, Witteveen-kolk syndrome

489
SIN3 transcription regulator family member B
-
Neurodevelopmental disorder, Witteveen-kolk syndrome

490
SIN3-HDAC complex associated factor
C12orf14, FAM60A, L4, TERA
Coronary artery disease, Non-small cell lung carcinoma, Pancreatic neoplasms, Diabetes mellitus type 2