Myh9<Gt(RRE342)Byg> Gene trapped Allele Detail MGI Mouse (MGI:3641195)

Myh9^{Gt(RRE342)Byg}
Gene trapped Allele Detail

Summary

Symbol:	Myh9^{Gt(RRE342)Byg}
Name:	myosin, heavy polypeptide 9, non-muscle; gene trap RRE342, BayGenomics
MGI ID:	MGI:3641195
Synonyms:	Myh9^{Gt(pGT2Lxf)4Byg}
Gene:	Myh9 Location: Chr15:77644788-77726315 bp, - strand Genetic Position: Chr15, 36.81 cM
Alliance:	Myh9^{Gt(RRE342)Byg} page

Mutation
origin

Mutant Cell Line:	RRE342
Germline Transmission:	Earliest citation of germline transmission: J:110432
Parent Cell Line:	Other (see notes) (ES Cell)
Strain of Origin:	129P2/OlaHsd

Mutation
description

Allele Type:

Gene trapped (Null/knockout, Reporter)

Mutation:

Insertion of gene trap vector Vector: pGT2Lxf Vector Type: gene trap

A gene trap vector, pGT2Lxf, containing a Betageo was inserted between exon 1 and 2. (J:110432)

Sequence Tags:

Sequence tag details (1 tag)

Genome Context:

Genome Browser view of this mutation

Phenotypes

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 Myh9 Mutation:	219 strains or lines available

Notes

All BayGenomics gene trap mutations were generated in either CGR8 or E14TG2a (129P2/OlaHsd) parental ES cell lines, with the majority in subline E14TG2a.4. The specific ES cell line in which each mutation was made is not specified.

References

Original:	J:110432 Parker LL, et al., Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: The use of public gene-targeted ES cell resources. Brain Res. 2006 May 26;1091(1):235-42
All:	2 reference(s)

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