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Barhl1tm1Xia
Targeted Allele Detail
Nomenclature
Symbol: Barhl1tm1Xia
Name: BarH like homeobox 1; targeted mutation 1, Mengqing Xiang
MGI ID: MGI:2181383
Synonyms: Barhl1-
Gene: Barhl1  Location: Chr2:28907679-28916668 bp, - strand  Genetic Position: Chr2, 19.38 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:77122
Parent Cell Line:  AB2.2 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprtb-m2
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe coding region of the gene was replaced with a lacZ/PGK-neo casette. The PGK-neo portion of the cassette is flanked by loxP sites. (J:77122)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 29 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Barhl1 Mutation:  12 strains or lines available
References
Original:  J:77122 Li S, et al., Hearing loss caused by progressive degeneration of cochlear hair cells in mice deficient for the Barhl1 homeobox gene. Development. 2002 Jul;129(14):3523-32
All:  4 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
04/06/2021
MGI 6.16
The Jackson Laboratory