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SLC9A1;jsessionid=DBD61CA45A8F05E6B5DA177159229349
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Accumbens
Salivary gland
Putamen
Parotid gland
Transverse colon
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Disease Atlas
Most Correlated Diseases
Pyloric ulcer
Pulmonary hypertension
Huntington's disease
Enteric campylobacteriosis
Eosinophilic disorder
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Pharmaco Atlas
Most Correlated Compounds
Amiloride
MK 0591
phorbolol-12-myristate-13-acetate
imidacloprid
graveoline
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Knockdown Atlas
Most Correlated Gene Perturbations
RBFOX1
SBDS
CLDN1
PC
GLS
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Slc9a1 plays a vital role in chitosan oligosaccharide transport across the intestinal mucosa of mice…
Role of Genetic Mutations of the Na+/H+ Exchanger Isoform 1, in Human Disease and Protein Targeting …
Overexpression of NHE1 suppresses ABCA1 protein expression via increasing calpain activity in RAW264…
Mutation of SLC9A1, encoding the major Na⁺/H⁺ exchanger, causes ataxia-deafness Lichtenstein-Knorr s…
Pharmacological Inhibition of NHE1 Protein Increases White Matter Resilience and Neurofunctional Rec…
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Clinical Trials
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There were no clinical trials for SLC9A1;jsessionid=DBD61CA45A8F05E6B5DA177159229349
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