decreased blood urea nitrogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description low circulating concentration of nitrogen, in the form of urea; commonly used to measure renal function (Mammalian Phenotype Ontology, MP_0005566)
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21 gene mutations causing the decreased blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BDKRB2 bradykinin receptor B2
CD44 CD44 molecule (Indian blood group)
CXCR3 chemokine (C-X-C motif) receptor 3
DDR2 discoidin domain receptor tyrosine kinase 2
DNASE1 deoxyribonuclease I
FAM117B family with sequence similarity 117, member B
HBP1 HMG-box transcription factor 1
IL1R1 interleukin 1 receptor, type I
MEP1B meprin A, beta
MIB2 mindbomb E3 ubiquitin protein ligase 2
NODAL nodal growth differentiation factor
RAPGEF3 Rap guanine nucleotide exchange factor (GEF) 3
SLC14A2 solute carrier family 14 (urea transporter), member 2
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
SMAD3 SMAD family member 3
SPSB2 splA/ryanodine receptor domain and SOCS box containing 2
SYK spleen tyrosine kinase
UBR1 ubiquitin protein ligase E3 component n-recognin 1
USP21 ubiquitin specific peptidase 21
WDR83 WD repeat domain 83
XXYLT1 xyloside xylosyltransferase 1