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 1631 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

851
Solute carrier family 9 member A1
APNH, LIKNS, NHE-1, NHE1, PPP1R143
Barrett esophagus, Cardiomyopathy, Cerebellar dysfunction with variable cognitive and behavioral abnormalities, Congestive heart failure, Experimental diabetes, Edema, Heart failure, Hypertrophic cardiomyopathy, Cerebellar ataxia with hearing loss, Ventricular remodeling

852
Solute carrier family 9 member A2
NHE2
Asthma, Eczema, Crohn disease, Dissection of aorta, Edema, Endometriosis, Leprosy, Respiratory system disease

853
Solute carrier family 9 member A3
DIAR8, NHE-3, NHE3
Autism, Congenital secretory diarrhea, Congenital sodium diarrhea, Cystic fibrosis, Experimental diabetes, Diarrhea, Diverticular disease, Dysentery, Edema, Hypotension, Intestinal obstruction, Lung disease, Schizophrenia

854
Solute carrier family 9 member A4
NHE4
Ankylosing spondylitis, Imperforate anus, Asthma, Eczema, Atypical femoral fracture, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Common variable immunodeficiency, Crohn disease, Dissection of aorta, Inflammatory bowel disease, Juvenile idiopathic arthritis, Leprosy, Nasal polyp
View all (6 more)

855
Solute carrier family 9 member A5
NHE5
Kidney failure

856
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

857
Solute carrier family 9 member A7
MRX108, NHE-7, NHE7, SLC9A6
Alzheimer disease, Intellectual developmental disorder, x-linked, X-linked intellectual disability

858
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

859
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

860
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