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Tbx22tm1.1Sta
Targeted Allele Detail
Nomenclature
Symbol: Tbx22tm1.1Sta
Name: T-box 22; targeted mutation 1.1, Philip Stanier
MGI ID: MGI:4361267
Synonyms: Tbx22null, Tbx22tm1.1(b-actin/Dexon0-2/NEO)Sta
Gene: Tbx22  Location: ChrX:107667964-107688978 bp, + strand  Genetic Position: ChrX, 47.59 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:153100
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129/Sv
Mutation
description
Allele Type:    Targeted (knock-out)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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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 Tbx22 Mutation:  3 strains or lines available
References
Original:  J:153100 Pauws E, et al., Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes. Hum Mol Genet. 2009 Nov 1;18(21):4171-9
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory