About   Help   FAQ
Symbol
Name
ID
Pex10
peroxisomal biogenesis factor 10
MGI:2684988
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties in infancy
Disease(s) Associated with PEX10
peroxisome biogenesis disorder 6A

Mouse Phenotypes
ataxia
abnormal prenatal movement
forelimb paralysis
hindlimb paralysis
Availability Mouse Genotype
Pex10m1Nisw/Pex10m1Nisw

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/19/2024
MGI 6.23
The Jackson Laboratory