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D17Aus9df27J
Radiation induced Allele Detail
Nomenclature
Symbol: D17Aus9df27J
Name: DNA segment, Chr 17, Austin 9; deficiency 27 Jackson
MGI ID: MGI:1857615
Gene: D17Aus9  Location: unknown  Genetic Position: Chr17, Syntenic
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:50247
Parent Cell Line:  v17.2 (ES Cell)
Strain of Origin:  (BALB/cJ x 129S4/SvJae)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Deletion
  D17Aus9df27J involves 13 genes/genome features (D17Aus9, Arid1b, Serac1 ...) View all
 
Mutation detailsThis mutation is a deletion that includes the D17Aus9 locus. It was generated by homologous recombination of a neomycin/thymidine kinase selection cassette into the D17Aus9 locus in ES cells, then irradiating these cells and selecting for cell lines that no longer expressed thymidine kinase. These ES cell lines were then used to create chimeric mice.
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 D17Aus9 Mutation:  2 strains or lines available
References
Original:  J:50247 Bergstrom RA, et al., Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths. Genetics. 1998 Oct;150(2):815-22
All:  1 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
10/08/2019
MGI 6.14
The Jackson Laboratory