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Ndntm1.1Mus
Targeted Allele Detail
Summary
Symbol: Ndntm1.1Mus
Name: necdin, MAGE family member; targeted mutation 1.1, Francoise Muscatelli
MGI ID: MGI:2653064
Gene: Ndn  Location: Chr7:61998025-61999676 bp, + strand  Genetic Position: Chr7, 34.36 cM, cytoband C
Alliance: Ndntm1.1Mus page
Increased apoptosis in the dorsal root ganglias of Ndntm1.1Mus/Ndn+ mice

Show the 3 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:66557
Parent Cell Line:  CK35 (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThe 5' two-thirds of the endogenous coding region was replaced with a floxed neo cassette inserted by homologous recombination. The neo cassette was then excised via cre-mediated recombination. (J:66557)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 121 assay results
In Structures Affected by this Mutation: 5 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 Ndn Mutation:  18 strains or lines available
References
Original:  J:66557 Muscatelli F, et al., Disruption of the mouse necdin gene results in hypothalamic and behavioral alterations reminiscent of the human prader-willi syndrome. Hum Mol Genet. 2000 Dec 12;9(20):3101-10
All:  10 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
03/12/2024
MGI 6.23
The Jackson Laboratory