abnormal urine nitrite level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the amount of nitrite (NO2-) in the urine; may be suggestive of impaired nitric oxide (NO) release, or of a urinary tract infection (Mammalian Phenotype Ontology, MP_0011740)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011740
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5 gene mutations causing the abnormal urine nitrite level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BDKRB2 bradykinin receptor B2
CYBB cytochrome b-245, beta polypeptide
NXPH4 neurexophilin 4
P2RX4 purinergic receptor P2X, ligand gated ion channel, 4
SLC14A2 solute carrier family 14 (urea transporter), member 2