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Derl2tm1.2Hpl
Targeted Allele Detail
Summary
Symbol: Derl2tm1.2Hpl
Name: Der1-like domain family, member 2; targeted mutation 1.2, Hidde Ploegh
MGI ID: MGI:4947129
Gene: Derl2  Location: Chr11:70898266-70910667 bp, - strand  Genetic Position: Chr11, 43.21 cM
Alliance: Derl2tm1.2Hpl page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:170650
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsCre-mediated recombination removed exons 4 through 6. The absence of protein expression was confirmed by western blot analysis on colon, pancreas, lymph node, spleen, thymus, lungs, liver, and lung extracts. (J:170650)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 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 Derl2 Mutation:  18 strains or lines available
References
Original:  J:170650 Dougan SK, et al., Derlin-2-deficient mice reveal an essential role for protein dislocation in chondrocytes. Mol Cell Biol. 2011 Mar;31(6):1145-59
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
10/22/2024
MGI 6.24
The Jackson Laboratory