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Mei1m1Jcs
Chemically induced Allele Detail
Summary
Symbol: Mei1m1Jcs
Name: meiotic double-stranded break formation protein 1; mutation 1, John C Schimenti
MGI ID: MGI:2176973
Synonyms: mei1, meiosis defective 1
Gene: Mei1  Location: Chr15:81954275-82011018 bp, + strand  Genetic Position: Chr15, 38.41 cM, cytoband E2
Alliance: Mei1m1Jcs page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:60747
Parent Cell Line:  CJ7 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Chemically induced (other)
Mutation:    Single point mutation
 
Mutation detailsThis mutation was identified in an EMS mutagenesis screen for infertile mice. The molecular defect is an A-to-T transversion at the AG splice acceptor sequence of intron 11. Two aberrantly spliced transcripts are expressed from this allele, both resulting in a frameshift of the wild-type sequence and a premature stop codon.
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 assay results
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Mei1 Mutation:  56 strains or lines available
References
Original:  J:60747 Munroe RJ, et al., Mouse mutants from chemically mutagenized embryonic stem cells. Nat Genet. 2000 Mar;24(3):318-21
All:  10 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
04/16/2024
MGI 6.23
The Jackson Laboratory