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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Grin3b
glutamate receptor, ionotropic, NMDA3B
MGI:2150393
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Grin3btm1b(KOMP)Wtsi/Grin3btm1b(KOMP)Wtsi
C57BL/6N-Grin3btm1b(KOMP)Wtsi/H
abnormal gait J:211773
decreased circulating fructosamine level J:211773
Grin3btm1Yaha/Grin3btm1Yaha
B6.129-Grin3btm1Yaha
abnormal motor capabilities/coordination/movement J:126239
abnormal social investigation J:126239
abnormal social/conspecific interaction J:126239
hypoactivity J:126239
impaired coordination J:126239
increased anxiety-related response J:126239
slow postnatal weight gain J:126239

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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last database update
11/30/2021
MGI 6.17
The Jackson Laboratory