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"
681 to 690 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

681
Solute carrier family 2 member 1
CSE, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT-1, GLUT1, GLUT1DS, HTLVR, PED, SDCHCN
Ataxia, Bell's palsy, Breast neoplasms, Ductal carcinoma, Hepatocellular carcinoma, Intraductal noninfiltrating carcinoma, Renal cell carcinoma, Cerebellar ataxia, Childhood absence epilepsy, Childhood-onset glut1 deficiency syndrome 2, Choreoathetosis, Chromosome 17q23.1-q23.2 deletion syndrome, Glucose transporter type 1 deficiency syndrome, Colonic neoplasms, Cryohydrocytosis
View all (25 more)

682
Solute carrier family 2 member 10
ATORS, ATS, GLUT10
Alzheimer disease, Androgenetic alopecia, Aortic aneurysm, Arterial tortuosity syndrome, Astrocytoma, Auditory system disease, Bicuspid aortic valve, Breast neoplasms, Color vision deficiency, Congenital contractural arachnodactyly, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Marfan syndrome, Orofacial cleft

683
Solute carrier family 2 member 11
GLUT10, GLUT11
Hypertrophic cardiomyopathy

684
Solute carrier family 2 member 12
GLUT12, GLUT8
Coronary artery disease, Oligodendroglioma, Open angle glaucoma, Prostate cancer, Scoliosis

685
Solute carrier family 2 member 13
HMIT
Alzheimer disease, Astrocytoma, Uinary system neoplasms, Colorectal cancer, Crohn disease, Inflammatory bowel disease, Insomnia, Leprosy, Parkinson disease, Progressive supranuclear palsy, Ulcerative colitis, Urogenital neoplasms

686
Solute carrier family 2 member 14
GLUT14, SLC2A3P3
Autism, Brain aneurysm, Parkinson disease

687
Solute carrier family 2 member 2
GLUT2
Breast neoplasms, Hepatocellular carcinoma, Experimental diabetes, Diabetes mellitus type 2, Diabetes mellitus permanent neonatal, Diabetic ketoacidosis, Long qt syndrome, Fanconi syndrome, Fanconi-bickel syndrome, Fatty liver, Fatty liver, alcoholic, Glycogen storage disease, Gout, Neonatal diabetes mellitus, Osteoarthritis

688
Solute carrier family 2 member 3
GLUT3
Alzheimer disease, Juvenile arthritis, Autism, Dementia, Allergic contact dermatitis, Huntington disease, Juvenile idiopathic arthritis, Lipidoses, Lipoidosis, Oligoarticular juvenile idiopathic arthritis

689
Solute carrier family 2 member 4
GLUT4
Alzheimer disease, Cardiomegaly, Experimental diabetes, Diabetes mellitus type 2, Hypertension, Hypothyroidism, Multiple sclerosis

690
SLC2A4 regulator
GEF, HDBP-1, HDBP1, Si-1-2, Si-1-2-19
Alzheimer disease, Asthma, Eczema, Gastroesophageal reflux disease, Multiple sclerosis, Prostate cancer