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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Grin3b
glutamate receptor, ionotropic, NMDA3B
MGI:2150393
12 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 triglyceride level J:211773
increased circulating bilirubin level J:211773
increased circulating potassium level J:211773
increased red blood cell distribution width J:211773
Grin3btm1Yaha/Grin3btm1Yaha
B6.129-Grin3btm1Yaha 		abnormal motor capabilities/coordination/movement J:126239
abnormal social investigation J:126239
abnormal social/conspecific interaction behavior J:126239
decreased locomotor activity 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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory