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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Grin2d
glutamate receptor, ionotropic, NMDA2D (epsilon 4)
MGI:95823
12 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Grin2dtm1a(EUCOMM)Wtsi/Grin2dtm1a(EUCOMM)Wtsi
Not Specified
abnormal bone mineralization J:165965
abnormal bone structure J:165965
decreased body weight J:165965
decreased circulating sodium level J:165965
decreased circulating triglyceride level J:165965
decreased heart weight J:165965
decreased lean body mass J:165965
Grin2dtm1Mim/Grin2dtm1Mim
B6.Cg-Grin2dtm1Mim
increased startle reflex J:89405
Grin2dtm1Mim/Grin2dtm1Mim
involves: C57BL/6 * CBA
normal behavior/neurological phenotype J:28825
decreased locomotor activity J:28825
decreased vertical activity J:28825
normal nervous system phenotype J:28825

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
04/16/2024
MGI 6.23
The Jackson Laboratory