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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nmur1
neuromedin U receptor 1
MGI:1341898
5 phenotypes from 5 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nmur1tm1.1(KOMP)Vlcg/Nmur1tm1.1(KOMP)Vlcg
C57BL/6N-Nmur1tm1.1(KOMP)Vlcg/Ucd
decreased caudal vertebrae number J:211773
Nmur1tm1Doma/Nmur1tm1Doma
B6N.Cg-Nmur1tm1Doma
normal homeostasis/metabolism phenotype J:152371
Nmur1tm1Lex/Nmur1tm1Lex
Not Specified
abnormal response/metabolism to endogenous compounds J:135815
Nmur1tm1Rtor/Nmur1tm1Rtor
involves: 129S6/SvEvTac * C57BL/6NCr * C57BL/6NTac
normal behavior/neurological phenotype J:124469
Nmur1tm1Sjab/Nmur1tm1Sjab
involves: 129P2/OlaHsd * C57BL/6
no abnormal phenotype detected J:142907

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory