Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "S"
761 to 770 of 1203 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

761
Solute carrier family 1 member 4
ASCT1, SATT, SPATCCM
Autism, Neurodevelopmental disorder, Macular telangiectasia, Non-specific syndromic intellectual disability

762
Solute carrier family 1 member 6
EAAT4
Bipolar disorder, Major depressive disorder, Schizophrenia, Squamous cell carcinoma, Depression

763
Solute carrier family 1 member 7
AAAT, EAAT5
Dementia, Systemic lupus erythematosus

764
Solute carrier family 2 member 1
CSE, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT-1, GLUT1, GLUT1DS, HTLVR, PED, SDCHCN
Ataxia, Bell's palsy, Breast neoplasm, 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, Colonic neoplasm, Developmental disability, Diabetes mellitus type 2
View all (23 more)

765
Solute carrier family 2 member 2
GLUT2
Breast neoplasm, Hepatocellular carcinoma, Experimental diabetes, Diabetes mellitus type 2, Diabetes mellitus permanent neonatal, Diabetic ketoacidosis, Long qt syndrome, Fatty liver, Fatty liver, alcoholic, Glycogen storage disease, Gout, Neonatal diabetes mellitus, Osteoarthritis, Diabetes mellitus, type 2

766
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

767
Solute carrier family 2 member 4
GLUT4
Alzheimer disease, Cardiomegaly, Experimental diabetes, Diabetes mellitus type 2, Hypertension, Hypothyroidism, Diabetes mellitus, type 2, Multiple sclerosis

768
Solute carrier family 2 member 5
GLUT-5, GLUT5
Breast neoplasm, Long qt syndrome

769
Solute carrier family 3 member 1
ATR1, CSNU1, D2H, NBAT, RBAT
Hypotonia-cystinuria syndrome, Autism, Cystinuria, Intellectual developmental disorder, Myasthenic syndrome, Nephrolithiasis

770
Solute carrier family 3 member 2
4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1, NACAE
Alzheimer disease, Autism, Insomnia, Lung neoplasms