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Mymxem1Shcs
Endonuclease-mediated Allele Detail
Summary
Symbol: Mymxem1Shcs
Name: myomixer, myoblast fusion factor; endonuclease-mediated mutation 1, Srihari C Sampath
MGI ID: MGI:5903202
Synonyms: Miniondelta
Gene: Mymx  Location: Chr17:45911897-45913028 bp, - strand  Genetic Position: Chr17, 22.59 cM
Alliance: Mymxem1Shcs page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9 technology introduced a 135 bp deletion in the single coding exon. Western blot analysis confirmed the absence of protein expression in limb and tongue at E16.5 and P0. (J:241565)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 9 assay results
In Structures Affected by this Mutation: 6 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Mymx Mutation:  28 strains or lines available
References
Original:  J:241565 Zhang Q, et al., The microprotein Minion controls cell fusion and muscle formation. Nat Commun. 2017 Jun 01;8:15664
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory