Mus musculus Gene: Pex19
Summary
InnateDB Gene IDBG-205149.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Pex19
Gene Name peroxisomal biogenesis factor 19
Synonyms Pxf
Species Mus musculus
Ensembl Gene ENSMUSG00000003464
Encoded Proteins
peroxisomal biogenesis factor 19
peroxisomal biogenesis factor 19
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000162735:
This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:172126755-172136493
Strand Forward strand
Band H3
Transcripts
ENSMUST00000075895 ENSMUSP00000075289
ENSMUST00000111252 ENSMUSP00000106883
ENSMUST00000147799
ENSMUST00000133546
ENSMUST00000127662
ENSMUST00000133081
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
They are also associated with 35 interaction(s) predicted by orthology.
Experimentally validated
Total 10 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 35 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0036105 peroxisome membrane class-1 targeting sequence binding
GO:0047485 protein N-terminus binding
GO:0051117 ATPase binding
Biological Process
GO:0006625 protein targeting to peroxisome
GO:0007031 peroxisome organization
GO:0016557 peroxisome membrane biogenesis
GO:0016559 peroxisome fission
GO:0045046 protein import into peroxisome membrane
GO:0050821 protein stabilization
GO:0061077 chaperone-mediated protein folding
GO:0072321 chaperone-mediated protein transport
GO:0072663 establishment of protein localization to peroxisome
GO:1900131 negative regulation of lipid binding
Cellular Component
GO:0005634 nucleus
GO:0005777 peroxisome
GO:0005778 peroxisomal membrane
GO:0005829 cytosol
GO:0016021 integral component of membrane
GO:0043231 intracellular membrane-bounded organelle
GO:0043234 protein complex
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
ABCA transporters in lipid homeostasis pathway
Transmembrane transport of small molecules pathway
ABC-family proteins mediated transport pathway
KEGG
Peroxisome pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
ABCA transporters in lipid homeostasis pathway
ABC-family proteins mediated transport pathway
Transmembrane transport of small molecules pathway
ABC-family proteins mediated transport pathway
ABCA transporters in lipid homeostasis pathway
Transmembrane transport of small molecules pathway
KEGG
Peroxisome pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.247764 Mm.474910 Mm.488816
RefSeq NM_001159525 NM_023041
OMIM
CCDS CCDS15508 CCDS48445
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas