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

Symbol:	Miatm1Rbu
Name:	MIA SH3 domain containing; targeted mutation1, Reinhard Buettner
MGI ID:	MGI:2159701
Synonyms:	MIA-, MIA/CD-RAP-
Gene:	Mia  Location: Chr7:26879166-26880574 bp, - strand  Genetic Position: Chr7, 15.84 cM
Alliance:	Miatm1Rbu page

Germline Transmission:	Earliest citation of germline transmission: J:74659
Parent Cell Line:	R1 (ES Cell)
Strain of Origin:	(129X1/SvJ x 129S1/Sv)F1-Kitl+

Allele Type:    Targeted (Null/knockout) Mutation:    Insertion   Mutation details: The neomycin cassette is inserted between exons 2 and 4. The allele encodes a truncated 57 amino acid protein.

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

In Mice Carrying this Mutation:

41 assay results

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 Mia Mutation:	15 strains or lines available

Original:	J:74659 Moser M, et al., Ultrastructural cartilage abnormalities in MIA/CD-RAP-deficient mice. Mol Cell Biol. 2002 Mar;22(5):1438-45
All:	3 reference(s)