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Rhoxtm1.1Wilk
Targeted Allele Detail
Summary
Symbol: Rhoxtm1.1Wilk
Name: reproductive homeobox cluster; targeted mutation 1.1, Miles F Wilkinson
MGI ID: MGI:5763218
Synonyms: Rhox-c-KO
Gene: Rhox  Location: unknown  Genetic Position: ChrX, Syntenic
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:229199
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intergenic deletion
  Rhoxtm1.1Wilk involves 50 genes/genome features (Rhox1, Rhox2a, Rhox3a ...) View all
 
Mutation detailsA loxP sites were inserted upstream of Rhox1 and into the second intron of Rhox13. Cre-mediated recombination removes the entire cluster. (J:229199)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
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 Rhox Mutation:  1 strain or line available
References
Original:  J:229199 Song HW, et al., shRNA off-target effects in vivo: impaired endogenous siRNA expression and spermatogenic defects. PLoS One. 2015;10(3):e0118549
All:  2 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
04/16/2024
MGI 6.23
The Jackson Laboratory