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"
851 to 860 of 1624 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

851
Solute carrier family 9 member A6
MRSA, MRXSCH, NDPACX, NHE6
Amblyopia, Astigmatism, Christianon syndrome, Global developmental delay, Hyperopia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Leukodystrophy, Neurodegenerative disorder, x-linked, female-restricted, with parkinsonism and cognitive impairment, Neurodevelopmental disorder, Scoliosis, Strabismus

852
Solute carrier family 9 member A7
MRX108, NHE-7, NHE7, SLC9A6
Alzheimer disease, Intellectual developmental disorder, x-linked, X-linked intellectual disability

853
Solute carrier family 9 member A8
NHE-8, NHE8
Amyotrophic lateral sclerosis, Ankylosing spondylitis, Coronary artery disease, Crohn disease, Dementia, Multiple sclerosis, Psoriasis, Psoriasis vulgaris, Sclerosing cholangitis, Ulcerative colitis

854
Solute carrier family 9 member A9
AUTS16, NHE9
Attention deficit hyperactivity disorder, Autism, Liver cirrhosis, Corneal ulcer, Coronary artery disease, Eosinophilia, Eye disease, Gout, Myocardial infarction, Nonalcoholic fatty liver disease, Penile disease, Rheumatoid arthritis, Sarcoidosis, Amyotrophic lateral sclerosis, Urinary system disease

855
Solute carrier family 9 member B1
NHA1, NHEDC1
Eczema, Atrial fibrillation, Cardiovascular disease, Hypertension, Migraine, Multiple sclerosis, Schizophrenia, Diabetes mellitus type 1, Diabetes mellitus type 2, Usher syndrome, Wolfram syndrome

856
Solute carrier family 9 member B2
NHA2, NHE10, NHEDC2
Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

857
Solute carrier family 9 member C1
NHE, NHE-10, SLC9A10, sperm-NHE
Oligodendroglioma

858
Solute carrier family 9 member C2 (putative)
NHE11, SLC9A11
Nephrotic syndrome, Nonalcoholic fatty liver disease, Psychiatric disorders, Scoliosis, Diabetes mellitus type 2

859
Solute carrier family 9 member D1
C13orf11, TMCO3
Basal cell carcinoma, Fuchs endothelial dystrophy

860
Solute carrier organic anion transporter family member 1A2
OATP, OATP-A, OATP1A2, SLC21A3
Asthma, Cholelithiasis, Myopathy, Progressive supranuclear palsy