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Gene: Anp32e MGI:1913721

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Gene Summary

Name:
acidic nuclear phosphoprotein 32 family member E
Synonyms:
LANP-L,  CPD1,  2810018A15Rik

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IMPC Data Collections

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 weight Anp32etm1e(KOMP)Wtsi HOM   Early adult 4.75×10-05

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.

Legacy Phenotype Associated Images
Anp32etm1e(KOMP)Wtsi
body, HOM, Male, WTSI
Anp32etm1e(KOMP)Wtsi
body, HOM, Male, WTSI
Anp32etm1e(KOMP)Wtsi
head, HOM, Male, WTSI
Anp32etm1e(KOMP)Wtsi
head, HOM, Male, WTSI
Anp32etm1e(KOMP)Wtsi
body, WT, Female, WTSI

View all 136 images

Anp32etm1e(KOMP)Wtsi
back skin, HOM, Female, WTSI
Anp32etm1e(KOMP)Wtsi
back skin, HOM, Female, WTSI
Anp32etm1e(KOMP)Wtsi
eye, fused cornea and lens, corneal opacity, HOM, Female, WTSI

Human diseases caused by Anp32e 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.

No human diseases associated to this gene by orthology or annotation.
No human diseases associated to this gene by phenotypic similarity.

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 Anp32e

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 Anp32e.

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

Title Journal IMPC Allele PubMed ID
Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis. Nature communications (August 2019) Anp32etm1e(KOMP)Wtsi PMC6671969
Mouse screen reveals multiple new genes underlying mouse and human hearing loss. PLoS biology (April 2019) Anp32etm1a(KOMP)Wtsi PMC6459510

Order Mouse and ES Cells

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
Anp32etm1e(KOMP)Wtsi Targeted, non-conditional allele Mice, ES Cells
Anp32etm1a(KOMP)Wtsi KO first allele (reporter-tagged insertion with conditional potential) Mice, Targeting vectors, ES Cells

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