Dataset | MPO Gene-Phenotype Associations |
Category | disease or phenotype associations |
Type | phenotype |
Description | an increased amount of creatinine in the urine compared to the normal state (Mammalian Phenotype Ontology, MP_0011470) |
External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011470 |
Similar Terms | |
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5 gene mutations causing the increased urine creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol | Name |
---|---|
CYBB | cytochrome b-245, beta polypeptide |
SLC12A1 | solute carrier family 12 (sodium/potassium/chloride transporter), member 1 |
SLC16A10 | solute carrier family 16 (aromatic amino acid transporter), member 10 |
SLC5A2 | solute carrier family 5 (sodium/glucose cotransporter), member 2 |
UMOD | uromodulin |