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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Nlrx1
NLR family member X1
MGI:2429611
12 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Nlrx1em1(IMPC)Mbp/Nlrx1em1(IMPC)Mbp
C57BL/6N-Nlrx1em1(IMPC)Mbp/MbpMmucd 		abnormal retina morphology J:211773
blind uterus J:211773
small spleen J:211773
Nlrx1tm1Jpyt/Nlrx1tm1Jpyt
involves: C57BL/6 * C57BL/6J 		abnormal macrophage physiology J:173995
abnormal neutrophil physiology J:173995
decreased body weight J:173995
increased circulating interleukin-6 level J:173995
increased interferon-beta secretion J:173995
increased interleukin-1 beta secretion J:173995
increased interleukin-6 secretion J:173995
increased susceptibility to endotoxin shock J:173995
increased susceptibility to Orthomyxoviridae infection J:173995
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory