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Chaer1em1Holi
Endonuclease-mediated Allele Detail
Summary
Symbol: Chaer1em1Holi
Name: cardiac hypertrophy associated epigenetic regulator 1; endonuclease-mediated mutation 1, Hongliang Li
MGI ID: MGI:5905817
Synonyms: Chaer1-KO
Gene: Chaer1  Location: Chr5:77283791-77288173 bp, - strand  Genetic Position: Chr5, Syntenic
Alliance: Chaer1em1Holi page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThis knockout allele was created by deleting exon 2 (which represents the bulk of the gene) using CRISPR/Cas9 technology. The sgRNAs flanking the exon were 5'-GTAGTTTGCACGTTAGCAAG-3' upstream and 5'-GATTACCGAGAACTGCCCGA-3' downstream. (J:240516)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Chaer1 Mutation:  0 strains or lines available
References
Original:  J:240516 Wang Z, et al., The long noncoding RNA Chaer defines an epigenetic checkpoint in cardiac hypertrophy. Nat Med. 2016 Oct;22(10):1131-1139
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
04/30/2024
MGI 6.23
The Jackson Laboratory