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"
671 to 680 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

671
Solute carrier family 27 member 3
ACSVL3, FATP3, VLCS-3
Respiratory system disease

672
Solute carrier family 27 member 4
ACSVL4, FATP4, IPS
Lamellar ichthyosis, Diabetes mellitus type 2

673
Solute carrier family 27 member 5
ACSB, ACSVL6, BACS, BAL, FACVL3, FATP-5, FATP5, VLACSR, VLCS-H2, VLCSH2
Colorectal cancer, Insomnia, Obesity

674
Solute carrier family 27 member 6
ACSVL2, FACVL2, FATP6, VLCS-H1
Alzheimer disease, Atrial fibrillation, Congenital right-sided heart lesions, Coronary artery disease, Hypertension, Heart failure, Insomnia, Myocardial infarction, Ocular sarcoidosis, Osteoarthritis, Ventricular fibrillation

675
Solute carrier family 28 member 1
CNT1, HCNT1, URCTU
Alzheimer disease, Breast neoplasms, Cerebral amyloid angiopathy, Color vision deficiency, Nephrolithiasis, Psoriasis, Retinal degeneration, Myopia, Uridine-cytidineuria

676
Solute carrier family 28 member 2
CNT2, HCNT2, HsT17153, SPNT1
Scoliosis

677
Solute carrier family 28 member 3
CNT3
Alzheimer disease, Androgenetic alopecia, Astrocytoma, Attention deficit hyperactivity disorder, Cannabis abuse, Color vision deficiency, Colorectal cancer, Diabetic retinopathy, Gout, Metabolic syndrome, Migraine, Multiple system atrophy, Obesity, Parkinson disease, Schizophrenia
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678
Solute carrier family 29 member 1 (Augustine blood group)
AUG, ENT1, hENT1
Fetal erythroblastosis, Huntington disease, Pancreatic neoplasms

679
Solute carrier family 29 member 3
ENT3, HCLAP, HJCD, PHID
Asthma, Congenital heart disease, Major depressive disorder, Desbuquois syndrome, Diabetes mellitus type 1, Digestive system neoplasms, Dyslipidemias, Hearing impairment, Hearing loss, Congenital heart defect, Hepatomegaly, Hypertrichosis, Hypogonadism, Obesity, Systemic lupus erythematosus
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680
Solute carrier family 29 member 4
ENT4, PMAT
Brain infarction, Cerebral amyloid angiopathy, Lewy body disease