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Bhlhe22tm2(cre)Gan
Targeted Allele Detail
Summary
Symbol: Bhlhe22tm2(cre)Gan
Name: basic helix-loop-helix family, member e22; targeted mutation 2, Lin Gan
MGI ID: MGI:3830517
Synonyms: Bhlh5cre
Gene: Bhlhe22  Location: Chr3:18108489-18111678 bp, + strand  Genetic Position: Chr3, 4.98 cM, cytoband A2
Alliance: Bhlhe22tm2(cre)Gan page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:144066
Parent Cell Line:  W4 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Recombinase)
Mutations:    Insertion, Intragenic deletion
 
Bhlhe22tm2(cre)Gan expression driven by 1 gene
    The coding region was replaced with a nuclear cre coding region. (J:144066)
Recombinase
activity
Activity:
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Driver: Bhlhe22 (mouse)
Summary of all recombinase alleles driven by Bhlhe22.
 

Phenotypes
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View phenotypes and curated references 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: 0 strains available      Cell Lines: 0 lines available
Carrying any Bhlhe22 Mutation:  12 strains or lines available
References
Original:  J:144066 Joshi PS, et al., Bhlhb5 regulates the postmitotic acquisition of area identities in layers II-V of the developing neocortex. Neuron. 2008 Oct 23;60(2):258-72
All:  5 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
04/16/2024
MGI 6.23
The Jackson Laboratory