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Nogtm1.1Rmh
Targeted Allele Detail
Summary
Symbol: Nogtm1.1Rmh
Name: noggin; targeted mutation 1.1, Richard M Harland
MGI ID: MGI:4941468
Synonyms: Nogfx
Gene: Nog  Location: Chr11:89191464-89193158 bp, - strand  Genetic Position: Chr11, 54.34 cM
Alliance: Nogtm1.1Rmh page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:169133
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA loxP site was placed upstream of the coding region of the Noggin (Nog) gene, and a FRT-flanked neomycin resistance (neo) cassette and a second loxP site were placed downstream. Flp-mediated recombination removed the neo cassette. (J:169133)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 66 assay results
In Structures Affected by this Mutation: 3 anatomical structure(s)
Find Mice (IMSR)
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 Nog Mutation:  18 strains or lines available
References
Original:  J:169133 Stafford DA, et al., Cooperative activity of noggin and gremlin 1 in axial skeleton development. Development. 2011 Mar;138(5):1005-14
All:  8 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
10/22/2024
MGI 6.24
The Jackson Laboratory