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Symbol
Name
ID
Pex19
peroxisomal biogenesis factor 19
MGI:1334458
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Disease(s) Associated with PEX19
peroxisome biogenesis disorder 12A

Mouse Phenotypes
abnormal embryo size
Availability Mouse Genotype
Pex19em1(IMPC)Bay/Pex19em1(IMPC)Bay

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
05/14/2024
MGI 6.23
The Jackson Laboratory