Symbol Name ID |
Grin2d
glutamate receptor, ionotropic, NMDA2D (epsilon 4) MGI:95823 |
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 |
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 12/10/2024 MGI 6.24 |
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