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Fgf5m2Btlr
Chemically induced Allele Detail
Summary
Symbol: Fgf5m2Btlr
Name: fibroblast growth factor 5; mutation 2, Bruce Beutler
MGI ID: MGI:5478737
Synonyms: splinter
Gene: Fgf5  Location: Chr5:98402108-98424892 bp, + strand  Genetic Position: Chr5, 47.77 cM, cytoband E1-F
Alliance: Fgf5m2Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsCapillary sequencing of the mutated gene identified a C to T transition at base pair 98261987 (v38) on chromosome 5 in the GenBank genomic region NC_000071 encoding Fgf5 (LOD = 4.56). The mutation corresponds to residue 394 in the mRNA sequence in exon 2 of 3 total exons. The mutation results in a substitution of arginine (R) to a premature stop codon at residue 132, and may cause nonsense-mediated decay of the transcript. (J:195411)
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 Fgf5 Mutation:  15 strains or lines available
References
Original:  J:195411 Beutler B, Direct Data Submission for splinter. MGI Direct Data Submission. 2013;v
All:  1 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