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Fendrrtm1Bgh
Targeted Allele Detail
Summary
Symbol: Fendrrtm1Bgh
Name: Foxf1 adjacent non-coding developmental regulatory RNA; targeted mutation 1, Bernhard G Herrmann
MGI ID: MGI:5470087
Synonyms: Fendrr3xpA[N]
Gene: Fendrr  Location: Chr8:121781621-121809849 bp, - strand  Genetic Position: Chr8, 70.28 cM
Alliance: Fendrrtm1Bgh page
Mutation
origin
Mouse Generated:  Earliest citation of chimera generation: J:191565
Parent Cell Line:  G4 (ES Cell)
Strain of Origin:  (129S6/SvEvTac x C57BL/6NCrl)F1
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 1 was replaced with an FRT flanked neo cassette and strong transcriptional stop signal via homologous recombination. (J:191565)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 2 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 Fendrr Mutation:  0 strains or lines available
References
Original:  J:191565 Grote P, et al., The Tissue-Specific lncRNA Fendrr Is an Essential Regulator of Heart and Body Wall Development in the Mouse. Dev Cell. 2013 Jan 28;24(2):206-14
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
12/10/2024
MGI 6.24
The Jackson Laboratory