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Scml2em1Shnk
Endonuclease-mediated Allele Detail
Summary
Symbol: Scml2em1Shnk
Name: Scm polycomb group protein like 2; endonuclease-mediated mutation 1, Satoshi H Namekawa
MGI ID: MGI:5690091
Synonyms: line 428
Gene: Scml2  Location: ChrX:159865521-160041209 bp, + strand  Genetic Position: ChrX, 73.95 cM
Alliance: Scml2em1Shnk page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsZinc finger endonucleases were used to generate a knock-out allele. Lines 428 contains an 8 base pair deletion in exon 6. Western blot analysis confirmed the absence of protein expression. (J:225041)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Scml2 Mutation:  13 strains or lines available
References
Original:  J:225041 Hasegawa K, et al., SCML2 establishes the male germline epigenome through regulation of histone H2A ubiquitination. Dev Cell. 2015 Mar 9;32(5):574-88
All:  7 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
10/29/2024
MGI 6.24
The Jackson Laboratory