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Slfn2m1Btlr
Chemically induced Allele Detail
Summary
Symbol: Slfn2m1Btlr
Name: schlafen 2; mutation 1, Bruce Beutler
MGI ID: MGI:3850348
Synonyms: elektra, Slfn2eka
Gene: Slfn2  Location: Chr11:82955938-82961504 bp, + strand  Genetic Position: Chr11, 50.3 cM
Alliance: Slfn2m1Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThis mutation comprises a T to A transversion at nucleotide position 586 of the gene (Genbank Accession NM_011408) that results in replacement of isoleucine by asparagine at amino acid position 135 of the protein (I135N). (J:158985)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Slfn2 Mutation:  14 strains or lines available
References
Original:  J:158985 Berger M, et al., An Slfn2 mutation causes lymphoid and myeloid immunodeficiency due to loss of immune cell quiescence. Nat Immunol. 2010 Apr;11(4):335-43
All:  4 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