Rnf212em1Amp
Endonuclease-mediated Allele Detail
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| 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
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| Alliance: |
Rnf212em1Amp page
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| Strain of Origin: |
(C57BL/6J x CBA/J)F2
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| Allele Type: |
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Endonuclease-mediated (Null/knockout) |
| Mutation: |
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Intragenic deletion
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Mutation details: CRISPR/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)
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| 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
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| Carrying any Rnf212 Mutation: |
11 strains or lines available
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| 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) |
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