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Ikbkaptm1.1Id
Targeted Allele Detail
Nomenclature
Symbol: Ikbkaptm1.1Id
Name: inhibitor of kappa light polypeptide enhancer in B cells, kinase complex-associated protein; targeted mutation 1.1, Ioannis Dragatsis
MGI ID: MGI:5297555
Synonyms: Ikbkapdelta20
Gene: Ikbkap  Location: Chr4:56749680-56802331 bp, - strand  Genetic Position: Chr4, 31.66 cM
Cardiovascular and brain malformations in Ikbkaptm1Id/Ikbkaptm1Id and Ikbkaptm1.1Id/Ikbkaptm1.1Id embryos

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:178070
Parent Cell Line:  W9.5/W95 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Generation of an Ikbkap allele lacking exon 20
Phenotypes
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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 Ikbkap Mutation:  8 strains or lines available
References
Original:  J:178070 Dietrich P, et al., Deletion of exon 20 of the familial dysautonomia gene ikbkap in mice causes developmental delay, cardiovascular defects, and early embryonic lethality. PLoS One. 2011;6(10):e27015
All:  2 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
12/09/2014
MGI 5.20
The Jackson Laboratory