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Gene: Pex16 MGI:1338829

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Gene Summary

Name:
peroxisomal biogenesis factor 16
Synonyms:
peroxisome biogenesis factor 16

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IMPC Data Collections

  • No Body Weight Data
  • No Embryo Imaging Data
  • No Viability Data

IMPC Phenotype Summary

Significant
Not Significant
Not tested

View all our phenotype data below

Phenotypes

The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.

Phenotype System Allele Zyg Sex Life Stage P Value
decreased body length Pex16tm1a(EUCOMM)Hmgu HET Early adult 8.34×10-05
preweaning lethality, complete penetrance Pex16tm1a(EUCOMM)Hmgu HOM   Early adult 0.00

Download data as:  TSV  XLS

Select physiological systems to view:
Viewing: all phenotypes
Select physiological systems to view:
Viewing: all phenotypes

lacZ Expression

Expression data not available

Associated Images

Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.

Phenotype associated images not available

Human diseases caused by Pex16 mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.

The table below shows human diseases associated to Pex16 by orthology or direct annotation.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Neonatal Adrenoleukodystrophy
ORPHA:44
Infantile Refsum Disease
ORPHA:772
Peroxisome Biogenesis Disorder 8A (Zellweger)
OMIM:614876
Peroxisome Biogenesis Disorder 8B
OMIM:614877
Zellweger Syndrome
ORPHA:912

The table below shows human diseases predicted to be associated to Pex16 by phenotypic similarity.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Neonatal Adrenoleukodystrophy
ORPHA:44
Infantile Refsum Disease
ORPHA:772
Peroxisome Biogenesis Disorder 8A (Zellweger)
OMIM:614876
Peroxisome Biogenesis Disorder 8B
OMIM:614877
Zellweger Syndrome
ORPHA:912

Histopathology

Summary table of phenotypes displayed during the Histopathology procedure which are considered significant. Full histopathology data table, including submitted images, can be accessed by clicking any row in this table.

There is no histopathology data for Pex16

IMPC related publications

The table below lists publications which used either products generated by the IMPC or data produced by the phenotyping efforts of the IMPC. These publications have also been associated to Pex16.

There are 2 publications which use IMPC produced mice or data.

Title Journal IMPC Allele PubMed ID
Loss of functional peroxisomes leads to increased mitochondrial biogenesis and reduced autophagy that preserve mitochondrial function. Cellular and molecular life sciences : CMLS (June 2023) Pex16tm1a(EUCOMM)Hmgu PMC10281899
Peroxisome-derived lipids regulate adipose thermogenesis by mediating cold-induced mitochondrial fission. The Journal of clinical investigation (January 2019) Pex16tm1a(EUCOMM)Hmgu 30511960

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All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.

MGI Allele Allele Type Produced
Pex16tm1a(EUCOMM)Hmgu KO first allele (reporter-tagged insertion with conditional potential) Mice, Targeting vectors, ES Cells
Pex16tm1e(EUCOMM)Hmgu Targeted, non-conditional allele ES Cells
Pex16tm1(KOMP)Vlcg Reporter-tagged deletion allele (with selection cassette) ES Cells

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