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Wlsem1Jgg
Endonuclease-mediated Allele Detail
Summary
Symbol: Wlsem1Jgg
Name: wntless WNT ligand secretion mediator; endonuclease-mediated mutation 1, Joseph G Gleeson
MGI ID: MGI:7541264
Synonyms: WlsY392C
Gene: Wls  Location: Chr3:159545309-159644300 bp, + strand  Genetic Position: Chr3, 82.65 cM
Alliance: Wlsem1Jgg page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Endonuclease-mediated (Humanized sequence)
Mutation:    Nucleotide substitutions
 
Mutation detailsCRISPR/Cas9 technology generated a tyrosine to cysteine substitution at amino acid 392 (p.Y392C). This is a pathogenic variant identified in children with Zaki syndrome consisting of multiorgan defects, microcephaly and facial dysmorphism. (J:341542)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
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 Wls Mutation:  38 strains or lines available
References
Original:  J:341542 Chai G, et al., A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. N Engl J Med. 2021 Sep 30;385(14):1292-1301
All:  1 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
12/10/2024
MGI 6.24
The Jackson Laboratory