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

Symbol:	Acvr1tm1.1Vk
Name:	activin A receptor, type 1; targeted mutation 1.1, Vesa Kaartinen
MGI ID:	MGI:3696672
Synonyms:	Acvr1fx(exon7), Alk2delta7
Gene:	Acvr1  Location: Chr2:58336450-58456840 bp, - strand  Genetic Position: Chr2, 33.05 cM
Alliance:	Acvr1tm1.1Vk page

Germline Transmission:	Earliest citation of germline transmission: J:73148
Parent Cell Line:	R1 (ES Cell)
Strain of Origin:	(129X1/SvJ x 129S1/Sv)F1-Kitl+

Allele Type:    Targeted (Null/knockout) Mutation:    Intragenic deletion     Exon 7 was removed via cre mediated recombination in Acvr1tm1Vk mutants. (J:73148)

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

In Mice Carrying this Mutation:	11 assay results
In Structures Affected by this Mutation:	31 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 Acvr1 Mutation:	44 strains or lines available

Original:	J:73148 Kaartinen V, et al., Removal of the floxed neo gene from a conditional knockout allele by the adenoviral Cre recombinase in vivo. Genesis. 2001 Nov;31(3):126-9
All:	7 reference(s)