Phenotypes for Gpr161 MGI:3775636 MGI Mouse

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Phenotypes Associated with This Genotype

Allelic Composition	Gpr161^vl/Gpr161^vl
Genetic Background	involves: C3H/HeSnJ * CAST/Ei

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gpr161^vl mutation (2 available); any Gpr161 mutation (30 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

behavior/neurological

hindlimb paralysis ( J:131929 )

• Background Sensitivity: seen in about 50% of adults on a mixed C3H/HeSnJ and C57BL/6J but never in adults on a pure C3H/HeSnJ background

nervous system

spina bifida ( J:131929 )

• Background Sensitivity: seen in about 50% of adults on a mixed C3H/HeSnJ and C57BL/6J but never in adults on a pure C3H/HeSnJ or a mixed C3H/HeSnJ and MOLF/Ei background

embryo

spina bifida ( J:131929 )

• Background Sensitivity: seen in about 50% of adults on a mixed C3H/HeSnJ and C57BL/6J but never in adults on a pure C3H/HeSnJ or a mixed C3H/HeSnJ and MOLF/Ei background

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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