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Symbol
Name
ID
Irf2bpl
interferon regulatory factor 2 binding protein-like
MGI:2442463
Phenotype annotations related to vision/eye
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
Availability Mouse Genotype
Irf2bplem1(IMPC)Bay/Irf2bpl+

Contributing Projects:
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
The Jackson Laboratory