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Gene: Megf10 MGI:2685177

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Not currently registered for phenotyping at IMPC

Phenotyping is currently not planned for a knockout strain of this gene.

Gene Summary

Name:
multiple EGF-like-domains 10
Synonyms:
LOC240312,  3000002B06Rik

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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.

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 Megf10 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 Megf10 by orthology or direct annotation.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Myopathy, Areflexia, Respiratory Distress, And Dysphagia, Early-Onset
Facial palsy OMIM:614399

The table below shows human diseases predicted to be associated to Megf10 by phenotypic similarity.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Retinal Dysplasia, Primary
Retinal dysplasia, Falciform retinal fold OMIM:312550
Lattice Degeneration Of Retina Leading To Retinal Detachment
Lattice retinal degeneration, Retinal detachment OMIM:150500
Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis
Cerebellar dysplasia, Cerebellar hypoplasia OMIM:616531
Retinal Detachment
Retinal detachment OMIM:180050
Coloboma Of Optic Nerve
Retinal detachment OMIM:120430
Chudley-Mccullough Syndrome
Cerebellar dysplasia, Cerebellar hypoplasia OMIM:604213
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 10
Cerebellar dysplasia OMIM:615041
Bilateral Frontoparietal Polymicrogyria
Abnormal cerebellum morphology, Cerebellar vermis hypoplasia, Cerebellar dysplasia, Hypoplasia of... ORPHA:101070
Crome Syndrome
Renal tubular epithelial necrosis, Cerebellar dysplasia OMIM:218900
Poretti-Boltshauser Syndrome
Cerebellar cyst, Dilated fourth ventricle, Cerebellar vermis hypoplasia, Cerebellar dysplasia OMIM:615960
Ataxia-Intellectual Disability-Oculomotor Apraxia-Cerebellar Cysts Syndrome
Cerebellar cyst, Cerebellar dysplasia, Dilated fourth ventricle, Inferior vermis hypoplasia, Elon... ORPHA:370022
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 5
Cerebellar cyst, Cerebellar dysplasia, Cerebellar hypoplasia, Dandy-Walker malformation, Hypoplas... OMIM:613153
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 11
Cerebellar cyst, Cerebellar dysplasia, Cerebellar hypoplasia, Hypoplasia of the pons OMIM:615181
3-Methylglutaconic Aciduria, Type Iv
Cerebellar dysplasia OMIM:250951
Mental Retardation, Autosomal Dominant 48
Cerebellar vermis hypoplasia, Cerebellar dysplasia, Cerebellar hypoplasia, Dilated fourth ventric... OMIM:617751
Muscular Dystrophy-Dystroglycanopathy (Congenital With Impaired Intellectual Impairment), Type B, 1
Cerebellar dysplasia, Cerebellar hypoplasia OMIM:613155
Joubert Syndrome 23
Cerebellar dysplasia OMIM:616490
Aprosencephaly And Cerebellar Dysgenesis
Poorly formed metencephalon, Cerebellar dysplasia OMIM:601374
Myopathy, Areflexia, Respiratory Distress, And Dysphagia, Early-Onset
Facial palsy OMIM:614399

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 Megf10

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 Megf10.

There are 3 publications which use IMPC produced mice or data.

Title Journal IMPC Allele PubMed ID
Formation of retinal direction-selective circuitry initiated by starburst amacrine cell homotypic contact. eLife (April 2018) Megf10tm1a(KOMP)Jrs Megf10tm1b(KOMP)Jrs PMC5931800
Megf10 Is a Receptor for C1Q That Mediates Clearance of Apoptotic Cells by Astrocytes. The Journal of neuroscience : the official journal of the Society for Neuroscience (May 2016) Megf10tm1(KOMP)Vlcg PMC4863057
Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways. Nature (November 2013) Megf10tm1(KOMP)Vlcg PMC3969024

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MGI Allele Allele Type Produced
Megf10tm42779(L1L2_st2) Targeting vectors
Megf10tm1(KOMP)Vlcg Reporter-tagged deletion allele (with selection cassette) Mice, Targeting vectors, ES Cells
Megf10tm42779(L1L2_Bact_P) Targeting vectors

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