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Sp8tm1Smb
Targeted Allele Detail
Summary
Symbol: Sp8tm1Smb
Name: trans-acting transcription factor 8; targeted mutation 1, Sheila M Bell
MGI ID: MGI:2684070
Synonyms: Sp8-
Gene: Sp8  Location: Chr12:118810064-118816311 bp, + strand  Genetic Position: Chr12, 63.48 cM
Alliance: Sp8tm1Smb page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:86196
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThe majority of the coding region, including the zinc finger domain, was deleted via cre mediated recombination of loxP sites in intron 2 and in the 3' untranslated region. (J:86196)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 110 assay results
In Structures Affected by this Mutation: 34 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 Sp8 Mutation:  29 strains or lines available
References
Original:  J:86196 Bell SM, et al., Sp8 is crucial for limb outgrowth and neuropore closure. Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12195-200
All:  9 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