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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Gpr161
G protein-coupled receptor 161
MGI:2685054
16 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Gpr161tm1Lex/Gpr161tm1Lex
involves: 129S/SvEv * C57BL/6N
abnormal craniofacial morphology J:193395
abnormal dorsal-ventral axis patterning J:193395
abnormal limb development J:193395
abnormal neural tube morphology J:193395
absent apical ectodermal ridge J:193395
normal embryo phenotype J:193395
embryonic lethality during organogenesis, complete penetrance J:193395
enlarged floor plate J:193395
exencephaly J:193395
spina bifida J:193395
Gpr161vl/Gpr161vl
C3Fe;C3Sn-Gpr161vl/J
abnormal neural fold formation J:2004
belly spot J:13464
cataract J:13464
normal hematopoietic system phenotype J:29151
spina bifida J:13464
vacuolated lens J:13464
Gpr161vl/Gpr161vl
involves: C3H/HeSnJ * C57BL/6J
hindlimb paralysis J:131929
spina bifida J:131929
Gpr161vl/Gpr161vl
involves: C3H/HeSnJ * CAST/Ei
hindlimb paralysis J:131929
spina bifida J:131929

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
11/07/2017
MGI 6.11
The Jackson Laboratory