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Rnlstm1Gvd
Targeted Allele Detail
Summary
Symbol: Rnlstm1Gvd
Name: renalase, FAD-dependent amine oxidase; targeted mutation 1, Gary V Desir
MGI ID: MGI:5433853
Gene: Rnls  Location: Chr19:33115147-33369665 bp, - strand  Genetic Position: Chr19, 29.08 cM
Alliance: Rnlstm1Gvd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:186878
Parent Cell Line:  W9.5/W95 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA neo cassette replaced exons 1 through 4. Western blot analysis confirmed the absence of protein expression in the kidney and heart. (J:186878)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Rnls Mutation:  21 strains or lines available
References
Original:  J:186878 Wu Y, et al., Renalase deficiency aggravates ischemic myocardial damage. Kidney Int. 2011 Apr;79(8):853-60
All:  7 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
10/29/2024
MGI 6.24
The Jackson Laboratory