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Genes Phenotypes Help, News, Blog

Gene: Praf2 MGI:1859607

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Gene Summary

Name:
PRA1 domain family 2
Synonyms:
Sfc20,  DXImx39e,  JM4

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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.

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

X-ray

XRay Images Forepaw

18 Images

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X-ray

XRay Images Skull Lateral Orientation

18 Images

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X-ray

XRay Images Whole Body Lateral Orientation

19 Images

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X-ray

XRay Images Whole Body Dorso Ventral

21 Images

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X-ray

XRay Images Skull Dorso Ventral Orientation

23 Images

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Legacy Phenotype Associated Images
Praf2tm1e(EUCOMM)Wtsi
HEMI, Male, WTSI
Praf2tm1e(EUCOMM)Wtsi
HEMI, Male, WTSI
Praf2tm1e(EUCOMM)Wtsi
HEMI, Male, WTSI
Praf2tm1e(EUCOMM)Wtsi
HEMI, Male, WTSI
Praf2tm1e(EUCOMM)Wtsi
HEMI, Male, WTSI

View all 99 images

Praf2tm1e(EUCOMM)Wtsi
cornea/lens fusion, HOM, Female, WTSI
Praf2tm1e(EUCOMM)Wtsi
abnormal retinal pigmentation, HEMI, Male, WTSI
Praf2tm1e(EUCOMM)Wtsi
right eye, HEMI, Male, WTSI
Praf2tm1e(EUCOMM)Wtsi
right eye, HEMI, Male, WTSI
Praf2tm1e(EUCOMM)Wtsi
abnormal cornea morphology, HEMI, Male, WTSI

View all 6 images

Praf2tm1e(EUCOMM)Wtsi
back skin, HOM, Female, WTSI

Human diseases caused by Praf2 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 Praf2

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 Praf2.

There are 4 publications which use IMPC produced mice or data.

Title Journal IMPC Allele PubMed ID
A Genome-Wide Screen in Mice To Identify Cell-Extrinsic Regulators of Pulmonary Metastatic Colonisation. G3 (Bethesda, Md.) (June 2020) Praf2tm1e(EUCOMM)Wtsi PMC7263671
Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis. Nature communications (August 2019) Praf2tm1e(EUCOMM)Wtsi PMC6671969
Mouse screen reveals multiple new genes underlying mouse and human hearing loss. PLoS biology (April 2019) Praf2tm1e(EUCOMM)Wtsi Praf2tm1e(EUCOMM)Wtsi PMC6459510
Genome wide in vivo mouse screen data from studies to assess host regulation of metastatic colonisation. Scientific data (September 2017) Praf2tm1e(EUCOMM)Wtsi PMC5827107

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
Praf2tm1e(EUCOMM)Wtsi Targeted, non-conditional allele Mice, ES Cells
Praf2tm1a(EUCOMM)Wtsi KO first allele (reporter-tagged insertion with conditional potential) Targeting vectors, ES Cells
Praf2tm1(KOMP)Vlcg Reporter-tagged deletion allele (with selection cassette) ES Cells

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