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"
651 to 660 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

651
Solute carrier family 25 member 45
-
Melanoma

652
Solute carrier family 25 member 46
HMSN6B, PCH1E
Asthma, Astrocytoma, Eczema, Charcot-marie-tooth disease, Congenital pontocerebellar hypoplasia, Hereditary motor and sensory neuropathies, Leigh syndrome, Major depressive disorder, Hereditary motor and sensory neuropathy, Optic atrophy, Pontocerebellar hypoplasia, Respiratory system disease, Retinitis pigmentosa, Seasonal allergic rhinitis, Spastic ataxia

653
Solute carrier family 25 member 47
C14orf68, HDCMP, HDMCP, HMFN1655
Hepatocellular carcinoma

654
Solute carrier family 25 member 48
-
Coronary aneurysm, Duchenne muscular dystrophy, Obesity, Prostate cancer, Schizophrenia, Scoliosis

655
Solute carrier family 25 member 5
2F1, AAC2, ANT2, T2, T3
Gout, Intellectual developmental disorder

656
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

657
Solute carrier family 26 member 11
-
Mucopolysaccharidosis, Stroke

658
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)

659
Solute carrier family 26 member 3
CLD, DRA
Cholecystolithiasis, Ulcerative colitis, Congenital chloride diarrhea, Congenital secretory diarrhea, Hydrops fetalis, Intestinal obstruction

660
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