Symbol Name ID |
Grin2b
glutamate receptor, ionotropic, NMDA2B (epsilon 2) MGI:95821 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Inguinal hernia |
Disease(s) Associated with GRIN2B | |
autosomal dominant intellectual developmental disorder 6 |
Mouse Phenotypes | enlarged heart |
growth/size/body region phenotype |
decreased body weight |
|
Availability | Mouse Genotype | |||
Grin2bem1Weya/Grin2bem1Weya | * | |||
Grin2btm1e.1(KOMP)Wtsi/Grin2b+ | ||||
Grin2btm1Mony/Grin2btm1Mony Tg(Camk2a-cre)1Gsc/0 (conditional) |
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 |
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