Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Barhl1tm1Xia
Name:	BarH like homeobox 1; targeted mutation 1, Mengqing Xiang
MGI ID:	MGI:2181383
Synonyms:	Barhl1-
Gene:	Barhl1  Location: Chr2:28797691-28806680 bp, - strand  Genetic Position: Chr2, 19.38 cM
Alliance:	Barhl1tm1Xia page

Germline Transmission:	Earliest citation of germline transmission: J:77122
Parent Cell Line:	AB2.2 (ES Cell)
Strain of Origin:	129S7/SvEvBrd-Hprt1b-m2

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion   Mutation details: The 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)

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:

70 assay results

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:	23 strains or lines available

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)