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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gpr17
G protein-coupled receptor 17
MGI:3584514
12 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Gpr17tm1(KOMP)Vlcg/Gpr17tm1(KOMP)Vlcg
C57BL/6NTac-Gpr17tm1(KOMP)Vlcg
normal no abnormal phenotype detected J:219560
Gpr17tm1Dgen/Gpr17tm1Dgen
B6.129-Gpr17tm1Dgen
increased vascular permeability J:150814
Gpr17tm1Qrlu/Gpr17tm1Qrlu
involves: 129S6/SvEvTac * C57BL/6
abnormal myelination J:154602
abnormal oligodendrocyte morphology J:154602
normal behavior/neurological phenotype J:154602
Tg(Cnp-Gpr17)1Qrlu/0
Not Specified
abnormal myelination J:154602
abnormal oligodendrocyte morphology J:154602
gliosis J:154602
hindlimb paralysis J:154602
microgliosis J:154602
normal nervous system phenotype J:154602
postnatal lethality J:154602
seizures J:154602
tremors J:154602

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