Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "S"
661 to 670 of 1624 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

661
Solute carrier family 26 member 5
DFNB61, PRES
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing impairment, Hearing loss, Nonsyndromic hearing loss

662
Solute carrier family 26 member 6
-
Hepatocellular carcinoma, Hyperoxaluria

663
Solute carrier family 26 member 7
SUT2
Congenital hypothyroidism, Hyperoxaluria, Schizophrenia, Upper aerodigestive tract neoplasm

664
Solute carrier family 26 member 8
AZON, SPGF3, TAT1
Nonobstructive azoospermia, Congenital impairment of spermatozoa motility, Diabetic foot, Schizophrenia, Spermatogenic failure

665
Solute carrier family 26 member 9
-
Cystic fibrosis, Cystic fibrosis-related diabetes, Diabetes mellitus, Intestinal obstruction, Lewy body disease, Diabetes mellitus type 2

666
Solute carrier family 27 member 3
ACSVL3, FATP3, VLCS-3
Respiratory system disease

667
Solute carrier family 27 member 4
ACSVL4, FATP4, IPS
Lamellar ichthyosis, Diabetes mellitus type 2

668
Solute carrier family 27 member 5
ACSB, ACSVL6, BACS, BAL, FACVL3, FATP-5, FATP5, VLACSR, VLCS-H2, VLCSH2
Colorectal cancer, Insomnia, Obesity

669
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

670
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