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Pgrem1Lvntu
Endonuclease-mediated Allele Detail
Summary
Symbol: Pgrem1Lvntu
Name: progesterone receptor; endonuclease-mediated mutation 1, Valerie Lin
MGI ID: MGI:6888212
Synonyms: PgR_AF1_QQQ
Gene: Pgr  Location: Chr9:8899834-8968612 bp, + strand  Genetic Position: Chr9, 2.46 cM
Alliance: Pgrem1Lvntu page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Not Specified)
Mutation:    Nucleotide substitutions
 
Mutation detailsCRISPR/Cas9 endonuclease-mediated genome editing is used to create amino acid substitutions at positions 461 (lysine to glutamine, K461Q, AAA to CAA), 478 (lysine to glutamine, K478Q, AAG to CAG), and 489 (arginine to glutamine, R489Q, CGG to CAG) located in the activation function 1 (AF1) domain. (J:326815)
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 Pgr Mutation:  73 strains or lines available
References
Original:  J:326815 Lee SH, et al., Activation function 1 of progesterone receptor is required for mammary development and regulation of RANKL during pregnancy. Sci Rep. 2022 Jul 19;12(1):12286
All:  2 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
04/30/2024
MGI 6.23
The Jackson Laboratory