Sequence Detail

ID/Version

O09012 Q3UM58 Q91YC7 Q8K2V5 (UniProt | EBI)

Last sequence update: 2007-04-03
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=Peroxisomal targeting signal 1 receptor {ECO:0000305}; Short=PTS1 receptor; Short=PTS1R;AltName: Full=PTS1-BP;AltName: Full=PXR1P;AltName: Full=Peroxin-5 {ECO:0000305};AltName: Full=Peroxisomal C-terminal targeting signal imp

Provider

SWISS-PROT

Sequence

Polypeptide 639 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Pex5	peroxisomal biogenesis factor 5	88	102	3	11

Sequence references in MGI

J:42719 Baes M, et al., A mouse model for Zellweger syndrome. Nat Genet. 1997 Sep;17(1):49-57
J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563
J:112503 Dirkx R, et al., Absence of peroxisomes in mouse hepatocytes causes mitochondrial and ER abnormalities. Hepatology. 2005 Apr;41(4):868-78
J:121804 Dirkx R, et al., Beta-oxidation in hepatocyte cultures from mice with peroxisomal gene knockouts. Biochem Biophys Res Commun. 2007 Jun 8;357(3):718-23
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89
J:319410 Ali M, et al., A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomes. Hum Genet. 2021 Apr;140(4):649-666