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Ncstntm1.2Sud
Targeted Allele Detail
Summary
Symbol: Ncstntm1.2Sud
Name: nicastrin; targeted mutation 1.2, Thomas C Sudhof
MGI ID: MGI:3848925
Gene: Ncstn  Location: Chr1:171893580-171910356 bp, - strand  Genetic Position: Chr1, 79.54 cM
Alliance: Ncstntm1.2Sud page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:149506
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsGerm line, cre mediated recombination removed exon 3. The absence of protein expression was confirmed by western blot analysis on fibroblast extracts. (J:149506)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Ncstn Mutation:  34 strains or lines available
References
Original:  J:149506 Tabuchi K, et al., Conditional forebrain inactivation of nicastrin causes progressive memory impairment and age-related neurodegeneration. J Neurosci. 2009 Jun 3;29(22):7290-301
All:  1 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
11/12/2024
MGI 6.24
The Jackson Laboratory