Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
741 to 750 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

741
ST3 beta-galactoside alpha-2,3-sialyltransferase 1
Gal-NAc6S, SIAT4A, SIATFL, ST3GalA, ST3GalA.1, ST3GalIA, ST3GalIA,1, ST3O
Bipolar disorder, Central nervous system cancer, Glioblastoma, Glioma, Non-organic psychosis, Non-small cell lung carcinoma, Psychotic disorders, Schizophrenia, Squamous cell carcinoma

742
ST3 beta-galactoside alpha-2,3-sialyltransferase 4
CGS23, NANTA3, SAT3, SIAT4, SIAT4C, ST-4, ST3GalA.2, ST3GalIV, STZ, gal-NAc6S
Androgenetic alopecia, Adenoid cystic carcinoma, Coronary artery disease, Hyperlipidemia, Hypertension, Leprosy, Metabolic syndrome, Salivary gland neoplasms, Venous thromboembolism

743
Solute carrier family 13 member 3
ARLIAK, NADC3, NaC3, SDCT2
Astrocytoma, Kidney disease, Gout, Diabetes mellitus, type 2

744
ST3 beta-galactoside alpha-2,3-sialyltransferase 3
DEE15, EIEE15, MRT12, SIAT6, ST3GALII, ST3Gal III, ST3GalIII, ST3N
Alzheimer disease, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Epilepsy due to perinatal stroke, Intellectual developmental disorder, Major depressive disorder, Migraine, Non-specific syndromic intellectual disability, Obesity, Peptic ulcer disease, Schizophrenia
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745
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
GD3S, SIAT8, SIAT8-A, SIAT8A, ST8SiaI
Attention deficit hyperactivity disorder, Liver cirrhosis, Dementia, Liver disease, Major depressive disorder, Nonalcoholic fatty liver disease, Diabetes mellitus, type 2

746
STIL centriolar assembly protein
MCPH7, SIL
Primary microcephaly, Congenital myasthenic syndrome, Holoprosencephaly, Intellectual developmental disorder, Microcephaly, Syntelencephaly, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Diabetes mellitus, type 2

747
SIM bHLH transcription factor 1
bHLHe14
Androgenetic alopecia, Atrial fibrillation, Bipolar disorder, Breast neoplasm, Venous insufficiency, Neurodevelopmental disorder, Erectile dysfunction, Heart failure, Hyperglycemia, Insomnia, Irritable bowel syndrome, Major depressive disorder, Intellectual developmental disorder, Metabolic syndrome, Neurotic disorder
View all (5 more)

748
Signal-induced proliferation-associated 1
SPA1
Eczema, Autoinflammatory disease, familial, behcet-like 3, Coronary artery disease, Esophageal atresia, Hypertension, Melanoma, Metabolic syndrome, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus, type 2

749
SIX homeobox 1
BOS3, DFNA23, TIP39
Isolated sensorineural deafness, Nonsyndromic hearing loss, Bor syndrome, Branchiootic syndrome, Branchiootorenal spectrum disorders, Branchio-oto-renal syndrome, Branchiootorenal syndrome, Congenital anomalies, Craniofacial abnormalities, Deafness, Endometrial neoplasm, Hearing impairment, Prostate cancer, Wilms tumor

750
SIX homeobox 3
HPE2
Anophthalmia/microphthalmia-esophageal atresia syndrome, Holoprosencephaly, Liver neoplasm, Lung cancer, Microform holoprosencephaly, Syntelencephaly, Schizencephaly, Schizophrenia, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Squamous cell carcinoma, Diabetes mellitus, type 2