| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Depletion of acid or accumulation base in the body fluids. (Human Phenotype Ontology, HP_0001948) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003028 |
| Similar Terms | |
| Downloads & Tools |
5 gene mutations causing the alkalosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| BSND | barttin CLCNK-type chloride channel accessory beta subunit |
| HIF1AN | hypoxia inducible factor 1, alpha subunit inhibitor |
| SCNN1B | sodium channel, non voltage gated 1 beta subunit |
| SLC12A1 | solute carrier family 12 (sodium/potassium/chloride transporter), member 1 |
| WNK4 | WNK lysine deficient protein kinase 4 |
