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