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Nkx2-1tm3Rdl
Targeted Allele Detail
Summary
Symbol: Nkx2-1tm3Rdl
Name: NK2 homeobox 1; targeted mutation 3, Roberto Di Lauro
MGI ID: MGI:4941952
Synonyms: Nkx2-1deltaCOOH
Gene: Nkx2-1  Location: Chr12:56578741-56583570 bp, - strand  Genetic Position: Chr12, 24.42 cM, cytoband C1-C3
Alliance: Nkx2-1tm3Rdl page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:169693
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe 3' coding region was removed and a neo cassette was inserted downstream of the coding region. The predicted protein product lacks the C-terminal amino acids (221-372). (J:169693)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 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 Nkx2-1 Mutation:  24 strains or lines available
References
Original:  J:169693 Silberschmidt D, et al., In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1. BMC Dev Biol. 2011;11:9
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
11/12/2024
MGI 6.24
The Jackson Laboratory