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Mstntm1.1Swel
Targeted Allele Detail
Summary
Symbol: Mstntm1.1Swel
Name: myostatin; targeted mutation 1.1, Stephen Welle
MGI ID: MGI:3620058
Synonyms: MstndeltaE3
Gene: Mstn  Location: Chr1:53100799-53107238 bp, + strand  Genetic Position: Chr1, 26.99 cM
Alliance: Mstntm1.1Swel page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:106054
Parent Cell Line:  AB1 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsExon 3, which encodes the entire active portion of the peptide, was removed via cre mediated recombination. (J:106054)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
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 Mstn Mutation:  34 strains or lines available
References
Original:  J:106054 Welle S, et al., Myofibrillar protein synthesis in myostatin-deficient mice. Am J Physiol Endocrinol Metab. 2006 Mar;290(3):E409-15
All:  3 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