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RlfMommeD8
Chemically induced Allele Detail
Summary
Symbol: RlfMommeD8
Name: rearranged L-myc fusion sequence; modifier of murine metastable epialleles, D8
MGI ID: MGI:3821599
Gene: Rlf  Location: Chr4:121003080-121072318 bp, - strand  Genetic Position: Chr4, 56.8 cM
Alliance: RlfMommeD8 page
Mutation
origin
Strain of Origin:  FVB/N
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsA G-to-T single point mutation in exon 8 is predicted to result in a C155F amino acid substitution in the encoded protein. Reduced amounts of encoded protein were detected on Western blot of embryonic tissue, suggesting that this allele is hypomorphic. (J:201508)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Rlf Mutation:  82 strains or lines available
References
Original:  J:142335 Ashe A, et al., A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development. Genome Biol. 2008 Dec 19;9(12):R182
All:  2 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
12/10/2024
MGI 6.24
The Jackson Laboratory