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Prmt1tm1Rchd
Targeted Allele Detail
Summary
Symbol: Prmt1tm1Rchd
Name: protein arginine N-methyltransferase 1; targeted mutation 1, Stephane Richard
MGI ID: MGI:3848226
Synonyms: Prmt1fl, PRMTFL
Gene: Prmt1  Location: Chr7:44626179-44635844 bp, - strand  Genetic Position: Chr7, 29.07 cM
Alliance: Prmt1tm1Rchd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:149155
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129/Sv
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted upstream of exon 4 and downstream of exon 5. A flp flanked neo cassette was removed by germ line, frt mediated recombination. (J:149155)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 2 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 16 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 Prmt1 Mutation:  35 strains or lines available
References
Original:  J:149155 Yu Z, et al., A mouse PRMT1 null allele defines an essential role for arginine methylation in genome maintenance and cell proliferation. Mol Cell Biol. 2009 Jun;29(11):2982-96
All:  14 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
11/19/2024
MGI 6.24
The Jackson Laboratory