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Prmt9em1Sqiu
Endonuclease-mediated Allele Detail
Summary
Symbol: Prmt9em1Sqiu
Name: protein arginine methyltransferase 9; endonuclease-mediated mutation 1, Shenfeng Qiu
MGI ID: MGI:8166513
Synonyms: Prmt9flox
Gene: Prmt9  Location: Chr8:78276026-78307967 bp, + strand  Genetic Position: Chr8, 36.61 cM
Alliance: Prmt9em1Sqiu page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Conditional ready)
Mutation:    Insertion
    Exon 5 was flanked by loxP sites via CRISPR/Cas9 technology. (J:360860)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Prmt9 Mutation:  29 strains or lines available
References
Original:  J:360860 Shen L, et al., Loss-of-function mutation in PRMT9 causes abnormal synapse development by dysregulation of RNA alternative splicing. Nat Commun. 2024 Apr 1;15(1):2809
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
03/18/2025
MGI 6.24
The Jackson Laboratory