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Sh3rf2tm1Zhxu
Targeted Allele Detail
Summary
Symbol: Sh3rf2tm1Zhxu
Name: SH3 domain containing ring finger 2; targeted mutation 1, Zhiheng Xu
MGI ID: MGI:6279851
Gene: Sh3rf2  Location: Chr18:42186732-42292025 bp, + strand  Genetic Position: Chr18, 22.21 cM
Alliance: Sh3rf2tm1Zhxu page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:270945
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Exon 1 was replaced by a lacZ expression cassette and a FRT-flanked neomycin resistance gene. (J:270945)
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: 1 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 Sh3rf2 Mutation:  53 strains or lines available
References
Original:  J:270945 Wang S, et al., Sh3rf2 Haploinsufficiency Leads to Unilateral Neuronal Development Deficits and Autistic-Like Behaviors in Mice. Cell Rep. 2018 Dec 11;25(11):2963-2971.e6
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
04/30/2024
MGI 6.23
The Jackson Laboratory