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Rnf212em1Amp
Endonuclease-mediated Allele Detail
Summary
Symbol: Rnf212em1Amp
Name: ring finger protein 212; endonuclease-mediated mutation 1, Alberto M Pendas
MGI ID: MGI:7281855
Synonyms: Rnf212-
Gene: Rnf212  Location: Chr5:108877156-108922848 bp, - strand  Genetic Position: Chr5, 53.24 cM
Alliance: Rnf212em1Amp page
Mutation
origin
Strain of Origin:  (C57BL/6J x CBA/J)F2
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9 technology generated a 142 bp deletion encompassing sequences in the end of exon 1, including the ATG start codon, and the start of intron 1 (GRCm39:chr5:108922731-108922872). (J:303558)
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 Rnf212 Mutation:  11 strains or lines available
References
Original:  J:303558 Felipe-Medina N, et al., A missense in HSF2BP causing primary ovarian insufficiency affects meiotic recombination by its novel interactor C19ORF57/BRME1. Elife. 2020 Aug 26;9:e56996
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
01/20/2026
MGI 6.24
The Jackson Laboratory