Peroxisomal biogenesis factor 19 is a protein that in humans is encoded by the PEX19 gene.
Interactions
PEX19 has been shown to interact with:
ABCD1, ABCD2, ABCD3, PEX10, PEX11B, PEX12, PEX13, PEX16, and PEX3.
References
Further reading
External links GeneReviews/NCBI/NIH/UW entry on Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum OMIM entries on Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum