Bos taurus Gene: PEX13
Summary
InnateDB Gene IDBG-634301.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PEX13
Gene Name Peroxisomal membrane protein PEX13
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000005257
Encoded Proteins
Peroxisomal membrane protein PEX13
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 ENSG00000162928:
This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 11:43608812-43640302
Strand Forward strand
Band
Transcripts
ENSBTAT00000006917 ENSBTAP00000006917
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 8 interaction(s) predicted by orthology.
Predicted by orthology
Total 8 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0001561 fatty acid alpha-oxidation
GO:0001764 neuron migration
GO:0001967 suckling behavior
GO:0006810 transport
GO:0007626 locomotory behavior
GO:0015031 protein transport
GO:0016560 protein import into peroxisome matrix, docking
GO:0021795 cerebral cortex cell migration
GO:0060152 microtubule-based peroxisome localization
Cellular Component
GO:0005777 peroxisome
GO:0005778 peroxisomal membrane
GO:0005779 integral component of peroxisomal membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
KEGG
Peroxisome pathway
Peroxisome pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Bt.57814
RefSeq NM_001076212
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas