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Sctrtm1Bkcc
Targeted Allele Detail
Summary
Symbol: Sctrtm1Bkcc
Name: secretin receptor; targeted mutation 1, Billy K C Chow
MGI ID: MGI:3711348
Synonyms: Sctr-
Gene: Sctr  Location: Chr1:119934710-119991269 bp, + strand  Genetic Position: Chr1, 52.57 cM
Alliance: Sctrtm1Bkcc page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:121376
Parent Cell Line:  AB2.2 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1b-m2
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 10, which encodes the third endoloop, was replaced with a PGK-neo cassette by homologous recombination. The loss of exon 10 resulted in a frameshift, thereby introducing a premature stop codon. The mutation is expected to be a null. (J:121376)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 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:121376 Chu JY, et al., Phenotypes developed in secretin receptor-null mice indicated a role for secretin in regulating renal water reabsorption. Mol Cell Biol. 2007 Apr;27(7):2499-511
All:  11 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