Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

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

Mouse Generated:	Earliest citation of chimera generation: J:191565
Parent Cell Line:	G4 (ES Cell)
Strain of Origin:	(129S6/SvEvTac x C57BL/6NCrl)F1

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: Exon 1 was replaced with an FRT flanked neo cassette and strong transcriptional stop signal via homologous recombination. (J:191565)

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	2 anatomical structure(s)

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

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)