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Prmt7tm1.2Rchd
Targeted Allele Detail
Summary
Symbol: Prmt7tm1.2Rchd
Name: protein arginine N-methyltransferase 7; targeted mutation 1.2, Stephane Richard
MGI ID: MGI:6281578
Gene: Prmt7  Location: Chr8:106937686-106978326 bp, + strand  Genetic Position: Chr8, 53.11 cM
Alliance: Prmt7tm1.2Rchd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:271361
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129/Sv
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExon 4 was flanked with loxP and FRT sites. Flp-mediated recombination removed the selection cassette inserted in intron 4. Cre-mediated recombination removed exon 4. (J:271361)
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Prmt7 Mutation:  41 strains or lines available
References
Original:  J:271361 Blanc RS, et al., PRMT7 Preserves Satellite Cell Regenerative Capacity. Cell Rep. 2016 Feb 16;14(6):1528-1539
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