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Hmcesem1Dfel
Endonuclease-mediated Allele Detail
Summary
Symbol: Hmcesem1Dfel
Name: 5-hydroxymethylcytosine (hmC) binding, ES cell specific; endonuclease-mediated mutation 1, Douglas E Feldman
MGI ID: MGI:6154268
Synonyms: Srap1 delta388
Gene: Hmces  Location: Chr6:87890917-87913611 bp, + strand  Genetic Position: Chr6, 39.13 cM
Alliance: Hmcesem1Dfel page
Mutation
origin
Strain of Origin:  (C57BL/6 x 129)F1
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCas9 mRNA and single-guide RNA (sgRNA) targeting exon 2 was microinjected into the cytoplasm of zygote-stage embryos to induce deletions. Injected embryos were implanted in CD-1 foster mice and pups screened for deletions. Two lines were generated. This allele has a 388 bp deletion encompassing the translation initiation codon and catalytic invariant Cys2 codon. (J:254234)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 assay results
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 Hmces Mutation:  19 strains or lines available
References
Original:  J:254234 Kweon SM, et al., Erasure of Tet-Oxidized 5-Methylcytosine by a SRAP Nuclease. Cell Rep. 2017 Oct 10;21(2):482-494
All:  3 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
04/23/2024
MGI 6.23
The Jackson Laboratory