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Ufd1ltm1Bld
Targeted Allele Detail
Nomenclature
Symbol: Ufd1ltm1Bld
Name: ubiquitin fusion degradation 1 like; targeted mutation 1, Antonio Baldini
MGI ID: MGI:3640091
Synonyms: Ufd1l-
Gene: Ufd1l  Location: Chr16:18811779-18835256 bp, + strand  Genetic Position: Chr16, 11.65 cM, cytoband B1-B4
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:57757
Parent Cell Line:  AB2.2 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprtb-m2
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsA targeting vector with the Hprt delta5' cassette and a loxP site was used to replace a 4.5kb region containing exons 2-3 of Ufd1l. The Udf1ltm1Bld mutant allele was created in the double-targeted cell line 217 which was originally derived from AB2.2 ES cells J:57757. (J:57757)
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Ufd1l Mutation:  19 strains or lines available
References
Original:  J:57757 Lindsay EA, et al., Congenital heart disease in mice deficient for the DiGeorge syndrome region [see comments]. Nature. 1999 Sep 23;401(6751):379-83
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
09/27/2016
MGI 6.05
The Jackson Laboratory