Symbol Name ID |
Grin2d
glutamate receptor, ionotropic, NMDA2D (epsilon 4) MGI:95823 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Disease(s) Associated with GRIN2D | |
developmental and epileptic encephalopathy 46 |
Mouse Phenotypes | abnormal bone structure |
abnormal bone mineralization |
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Availability | Mouse Genotype | ||
Grin2dtm1a(EUCOMM)Wtsi/Grin2dtm1a(EUCOMM)Wtsi |
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 05/14/2024 MGI 6.23 |
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