Bos taurus Gene: PEX19
Summary
InnateDB Gene IDBG-630601.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PEX19
Gene Name Peroxisomal biogenesis factor 19
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000007537
Encoded Proteins
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 3:9517705-9523145
Strand Forward strand
Band
Transcripts
ENSBTAT00000009921 ENSBTAP00000009921
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 35 interaction(s) predicted by orthology.
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:0005737 cytoplasm
GO:0005777 peroxisome
GO:0005778 peroxisomal membrane
GO:0005829 cytosol
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0043231 intracellular membrane-bounded organelle
GO:0043234 protein complex
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
ABC-family proteins mediated transport pathway
ABCA transporters in lipid homeostasis pathway
Transmembrane transport of small molecules pathway
KEGG
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
ABCA transporters in lipid homeostasis pathway
Transmembrane transport of small molecules pathway
ABC-family proteins mediated transport pathway
KEGG
Peroxisome pathway
Peroxisome pathway
INOH
PID NCI
Cross-References
SwissProt Q3SZD1
TrEMBL
UniProt Splice Variant
Entrez Gene 521522
UniGene Bt.46094
RefSeq NM_001034540
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC102949
GenPept AAI02950
RNA Seq Atlas 521522