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Sctrtm1Brd
Targeted Allele Detail
Summary
Symbol: Sctrtm1Brd
Name: secretin receptor; targeted mutation 1, Allan Bradley
MGI ID: MGI:5774826
Synonyms: Sctrm1Brd
Gene: Sctr  Location: Chr1:119934710-119991269 bp, + strand  Genetic Position: Chr1, 52.57 cM
Alliance: Sctrtm1Brd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:114853
Parent Cell Line:  AB2.2 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA beta-galactosidase and neomycin resistance cassette replaced exon 1. RT-PCR confirmed the absence of protein expression in cerebrum, cerebellum, pancreas, heart, liver, kidney, lung, intestine, stomach, spleen and muscle. (J:114853)
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 Sctr Mutation:  27 strains or lines available
References
Original:  J:114853 Nishijima I, et al., Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior. Hum Mol Genet. 2006 Nov 1;15(21):3241-50
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
04/16/2024
MGI 6.23
The Jackson Laboratory