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

Symbol:	Htr1ftm1.1(KOMP)Vlcg
Name:	5-hydroxytryptamine (serotonin) receptor 1F; targeted mutation 1.1, Velocigene
MGI ID:	MGI:5520176
Gene:	Htr1f  Location: Chr16:64745092-64926147 bp, - strand  Genetic Position: Chr16, 37.1 cM
Alliance:	Htr1ftm1.1(KOMP)Vlcg page
IMPC:	Htr1f gene page

Mutant Cell Line:	13331A-E12
Germline Transmission:	Earliest citation of germline transmission: J:188991
Parent Cell Line:	VGB6 (ES Cell)
Strain of Origin:	C57BL/6NTac
Project Collection:	KOMP-Regeneron

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion     Vector: ZEN-Ub1   Mutation details: The insertion of Velocigene cassette ZEN-Ub1 created a deletion of size 1119bp between positions 64925632-64926750 of Chromosome 16 (Genome Build37) and subsequent Cre-mediated deletion excised the neomycin selection cassette. (J:136110, J:188991)

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

In Mice Carrying this Mutation:	17 assay results
In Structures Affected by this Mutation:	1 anatomical structure(s)

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Htr1f Mutation:	28 strains or lines available

Original:	J:188991 The Jackson Laboratory, Alleles produced for the KOMP project by The Jackson Laboratory. MGI Direct Data Submission. 2012;
All:	6 reference(s)