Symbol Name ID |
Irf2bpl
interferon regulatory factor 2 binding protein-like MGI:2442463 |
Darker colors indicate more annotations |
Human Phenotypes | Esotropia |
Nystagmus |
Disease(s) Associated with IRF2BPL | ||
neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures |
Mouse Phenotypes | abnormal eye posterior chamber depth |
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Availability | Mouse Genotype | |
Irf2bplem1(IMPC)Bay/Irf2bpl+ |
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 04/30/2024 MGI 6.23 |
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