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Nf2tm2.1Gth
Targeted Allele Detail
Summary
Symbol: Nf2tm2.1Gth
Name: neurofibromin 2; targeted mutation 2.1, Gilles Thomas
MGI ID: MGI:1926957
Synonyms: Nf2delta2
Gene: Nf2  Location: Chr11:4715845-4799536 bp, - strand  Genetic Position: Chr11, 3.0 cM
Alliance: Nf2tm2.1Gth page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:63264
Parent Cell Line:  HM-1 (ES Cell)
Strain of Origin:  129P2/OlaHsd-Hprt1b-m3
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThis allele is a derivative of Nf2tm2Gth in which a Cre mediated recombination event in the germline removed exon 2. (J:63264)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Tumor Data
List all tumor models in MMHCdb carrying Nf2tm2.1Gth
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 Nf2 Mutation:  65 strains or lines available
References
Original:  J:63264 Giovannini M, et al., Conditional biallelic Nf2 mutation in the mouse promotes manifestations of human neurofibromatosis type 2. Genes Dev. 2000 Jul 1;14(13):1617-30
All:  4 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
04/23/2024
MGI 6.23
The Jackson Laboratory