banner
Genes Phenotypes Help, News, Blog

Gene: Mndal MGI:3780953

Log in to follow

Gene Summary

Name:
myeloid nuclear differentiation antigen like
Synonyms:
Ifi212

Order Alleles

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
abnormal embryo size Mndalem1(IMPC)Bay HET E12.5 0.00
preweaning lethality, complete penetrance Mndalem1(IMPC)Bay HOM   Early adult 0.00
preweaning lethality, complete penetrance Mndalem1(IMPC)Wtsi HOM   Early adult 7.54×10-06
abnormal embryo size Mndalem1(IMPC)Bay HET E9.5 0.00
abnormal gait Mndalem1(IMPC)Wtsi HET   Early adult 1.44×10-05

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.

Eye Morphology

VIP of right eye

17 Images

View images
Eye Morphology

VIP of left fundus

17 Images

View images
Eye Morphology

VIP of left eye

17 Images

View images
Eye Morphology

VIP of right fundus

17 Images

View images
Download thumbnail Download
MicroCT E9.5

Embryo reconstruction

2 Images

View images

Human diseases caused by Mndal 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.

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

Disease Similarity of
phenotypes		 Matching phenotypes Source
Psychogenic Movement Disorders
Gait disturbance ORPHA:71519
Benign Hereditary Chorea
Gait disturbance ORPHA:1429
Vertigo, Benign Recurrent
Gait imbalance OMIM:193007
Ataxia-Oculomotor Apraxia Type 1
Ataxia, Gait disturbance ORPHA:1168
Early-Onset Generalized Limb-Onset Dystonia
Gait disturbance ORPHA:256

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 Mndal

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 Mndal.

No publications found that use IMPC mice or data for Mndal.

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
Mndalem1(IMPC)Wtsi Exon Deletion Mice
Mndalem1(IMPC)Bay Exon Deletion Mice

The IMPC Newsletter

Get highlights of the most important data releases, news and events, delivered straight to your email inbox

Subscribe to newsletter