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Rlimtm1.2Inba
Targeted Allele Detail
Nomenclature
Symbol: Rlimtm1.2Inba
Name: ring finger protein, LIM domain interacting; targeted mutation 1.2, Ingol Bach
MGI ID: MGI:4838154
Synonyms: Rnf12delta
Gene: Rlim  Location: ChrX:103957163-103981284 bp, - strand  Genetic Position: ChrX, 46.42 cM, cytoband D
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:165550
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsCre mediated recombination removed the coding region of exon 5 and the inserted neo cassette. The absence of protein expression was confirmed by western blot analysis on brain and breast extracts from male mice. (J:165550)
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 Rlim Mutation:  14 strains or lines available
References
Original:  J:165550 Shin J, et al., Maternal Rnf12/RLIM is required for imprinted X-chromosome inactivation in mice. Nature. 2010 Oct 21;467(7318):977-81
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory