Symbol Name ID |
Pex2
peroxisomal biogenesis factor 2 MGI:107486 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatosplenomegaly |
Hepatomegaly |
Failure to thrive |
Small for gestational age |
Intrauterine growth retardation |
Disease(s) Associated with PEX2 | ||||||
peroxisome biogenesis disorder 5A |
Mouse Phenotypes | decreased embryo weight |
microcephaly |
postnatal growth retardation |
|
Availability | Mouse Genotype | |||
Pex2tm1Plf/Pex2tm1Plf |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 09/03/2024 MGI 6.24 |
|
|