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"
661 to 670 of 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

661
Solute carrier family 26 member 1
CAON, CAON1, EDM4, HYSULF, SAT-1, SAT1
Alzheimer disease, Developmental and epileptic encephalopathy, Hyperoxaluria, Mucopolysaccharidosis, Nephrolithiasis, Pfaundler-hurler syndrome, Polymyositis, Urolithiasis

662
Solute carrier family 26 member 11
-
Mucopolysaccharidosis, Stroke

663
Solute carrier family 26 member 2
D5S1708, DTD, DTDST, EDM4, MST153, MSTP157
Achondrogenesis, Atelosteogenesis, Bone disease, Brachydactyly, Carnevale syndrome, Congenital cartilage disorder, Connective tissue disease, Craniofacial abnormalities, De la chapelle dysplasia, Desbuquois syndrome, Diastrophic dysplasia, Diastrophic dysplasia, broad bone-platyspondylic variant, Ear disease, Epiphyseal dysplasia, Juvenile idiopathic arthritis
View all (4 more)

664
Solute carrier family 26 member 3
CLD, DRA
Cholecystolithiasis, Ulcerative colitis, Congenital chloride diarrhea, Congenital secretory diarrhea, Dysentery, Hydrops fetalis, Intestinal obstruction

665
Solute carrier family 26 member 4
DFNB4, EVA, PDS, TDH2B
Congenital hypothyroidism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Thyroid agenesis, Congenital ear anomaly, Congenital hypothyroidism due to absence of thyroid gland, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Pendred syndrome, Prostatic neoplasms, Wolff-parkinson-white syndrome

666
Solute carrier family 26 member 5
DFNB61, PRES
Isolated sensorineural deafness, Nonsyndromic intellectual disability, Deafness, Hearing impairment, Hearing loss, Nonsyndromic hearing loss

667
Solute carrier family 26 member 6
-
Hepatocellular carcinoma, Hyperoxaluria

668
Solute carrier family 26 member 7
SUT2
Congenital hypothyroidism, Hyperoxaluria, Schizophrenia, Upper aerodigestive tract neoplasm

669
Solute carrier family 26 member 8
AZON, SPGF3, TAT1
Nonobstructive azoospermia, Congenital impairment of spermatozoa motility, Diabetic foot, Schizophrenia, Spermatogenic failure

670
Solute carrier family 26 member 9
-
Cystic fibrosis, Diabetes mellitus, Intestinal obstruction, Lewy body disease, Diabetes mellitus type 2