About   Help   FAQ
Bhlhe22tm2.1Meg
Targeted Allele Detail
Nomenclature
Symbol: Bhlhe22tm2.1Meg
Name: basic helix-loop-helix family, member e22; targeted mutation 2.1, Michael E Greenberg
MGI ID: MGI:4440744
Synonyms: Bhlhb5fl
Gene: Bhlhe22  Location: Chr3:18054325-18057514 bp, + strand  Genetic Position: Chr3, 4.98 cM, cytoband A2
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:158273
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129/Sv
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
    LoxP sites flank the single coding exon of this gene. (J:158273)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structures
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:  8 strains or lines available
References
Original:  J:158273 Ross SE, et al., Loss of inhibitory interneurons in the dorsal spinal cord and elevated itch in Bhlhb5 mutant mice. Neuron. 2010 Mar 25;65(6):886-98
All:  3 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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/10/2019
MGI 6.14
The Jackson Laboratory