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Lmnb1tm2Sgy
Targeted Allele Detail
Summary
Symbol: Lmnb1tm2Sgy
Name: lamin B1; targeted mutation 2, Stephen G Young
MGI ID: MGI:5517592
Synonyms: Lmnb1CS
Gene: Lmnb1  Location: Chr18:56840885-56886496 bp, + strand  Genetic Position: Chr18, 30.84 cM
Alliance: Lmnb1tm2Sgy page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:197315
Parent Cell Line:  E14TG2a (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted
Mutation:    Insertion
 
Mutation detailsThe TGT cysteine codon of the CaaX motif was changed to a TCT serine codon. In addition, a floxed neo resistance cassette was introduced 1.5 kb downstream of the point mutation. (J:197315)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 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 Lmnb1 Mutation:  38 strains or lines available
References
Original:  J:197315 Jung HJ, et al., Farnesylation of lamin B1 is important for retention of nuclear chromatin during neuronal migration. Proc Natl Acad Sci U S A. 2013 May 21;110(21):E1923-32
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
04/23/2024
MGI 6.23
The Jackson Laboratory