Gene Summary

Name:
myelin regulatory factor
Synonyms:
Gm98,  LOC386531,  LOC225908

IMPC Data Collections

IMPC Phenotype Summary

Significant
Not Significant
Not tested

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
abnormal embryo turning Myrfem1(IMPC)Bay HOM E9.5 0.00
abnormal embryo size Myrfem1(IMPC)Bay HOM E9.5 0.00
abnormal embryo size Myrfem1(IMPC)Bay HET E12.5 0.00
preweaning lethality, complete penetrance Myrfem1(IMPC)Bay HOM   Early adult 0.00
embryonic lethality prior to tooth bud stage Myrfem1(IMPC)Bay HOM   E12.5 0.00
embryonic growth retardation Myrfem1(IMPC)Bay HOM E9.5 0.00
embryonic growth retardation Myrfem1(IMPC)Bay HET E12.5 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.

Eye Morphology

VIP of left eye

16 Images

Eye Morphology

VIP of right fundus

16 Images

Eye Morphology

VIP of right eye

16 Images

Eye Morphology

VIP of left fundus

16 Images

Human diseases caused by Myrf 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 Myrf by orthology or direct annotation.

Disease Similarity of
phenotypes
Matching phenotypes Source
Cardiac-Urogenital Syndrome
Patent urachus OMIM:618280
Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization
OMIM:618113

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

Disease Similarity of
phenotypes
Matching phenotypes Source
Cardiac-Urogenital Syndrome
Patent urachus OMIM:618280
Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization
OMIM:618113

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 Myrf

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 Myrf.

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) Myrfltm1a(EUCOMM)Wtsi PMC6671969
Mouse screen reveals multiple new genes underlying mouse and human hearing loss. PLoS biology (April 2019) Myrfltm1a(EUCOMM)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
Myrftm1(NCOM)Cmhd Reporter-tagged deletion allele (with selection cassette) Targeting vectors, ES Cells
Myrfem1(IMPC)Bay Exon Deletion Mice

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