Grin3b Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Grin3b^{tm1b(KOMP)Wtsi}/Grin3b^{tm1b(KOMP)Wtsi} C57BL/6N-Grin3b^{tm1b(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
Grin3b^tm1Yaha/Grin3b^tm1Yaha B6.129-Grin3b^tm1Yaha	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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