Symbol Name ID |
Grin2d
glutamate receptor, ionotropic, NMDA2D (epsilon 4) MGI:95823 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Drooling |
Decreased fetal movement |
Feeding difficulties |
Disease(s) Associated with GRIN2D | |||
developmental and epileptic encephalopathy 46 |
Mouse Phenotypes | behavior/neurological phenotype |
increased startle reflex |
decreased vertical activity |
decreased locomotor activity |
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Availability | Mouse Genotype | ||||
Grin2dtm1Mim/Grin2dtm1Mim | * |
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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