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Fgfr2svs
Spontaneous Allele Detail

Nomenclature
Symbol: Fgfr2svs
Name: fibroblast growth factor receptor 2; seminal vesicle shape
MGI ID: MGI:1856633
Synonyms: svs
Gene: Fgfr2   Location: Chr7:137305965-140315033 bp, - strand    Genetic Position: Chr7, 62.0 cM
Mutation
origin
Strain of Origin: CXB5/By
Mutation
description
Allele Type: Spontaneous
Mutation: Viral insertion
  An insertion of a 491-bp mouse leukemia virus long terminal repeat (MLV-LTR) sequence into intron 10 results in aberrant alternative splicing of the transcript with exclusion from most mature mutant mRNA species of exon 8IIIb, which encodes the domain required for specific binding to FGF ligands in developing prostate and seminal vesicle mesenchyme. (J:119935)
Inheritance: Recessive
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 Fgfr2 Mutation: 16 strains or lines available
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

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Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
hm1
 
ht2
 
ht3
  
endocrine/exocrine glands          
N
  
reproductive system          
 
Phenotypic
data by
genotype
Phenotypic Data by Genotype

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GenotypeAllelic CompositionGenetic Background
  
 hm1   
Fgfr2svs/Fgfr2svs involves: CXB5/ByJ
  
 ht2   
Fgfr2tm1Dor/Fgfr2svs involves: 129X1/SvJ * CXB5/ByJ * FVB/N
  
 ht3   
Fgfr2tm1.1Dor/Fgfr2svs involves: 129X1/SvJ * CXB5/ByJ * FVB/N
Notes Seminiferous tubules in male mice of the CXBI/ByEss recombinant inbred strain were found to be tubular and smooth, in contrast to normal mice such as C57BL/6By males, in which the seminal vesicles are curved and convoluted. A recessive autosomal mutation apparently occurred early in the inbreeding of the CXB recombinant inbred lines, as the abnormality was not present in either of the parental strains, C57BL/6ByEss or BALB/cByEss, but is present in both CXBI/ByJax and CXBI/ByLac. The mutation has been given the name and symbol seminal vesicle shape, svs. It appears to be linked to Tyr on Chr 7. In segregating crosses, svs/svs homozygotes had slightly lighter seminal vesicles than normal, though the weights of other androgen target organs were not reduced. Seminal vesicles responded to exogenous testosterone by increased size, but their shape did not change. The protein pattern under SDS--acrylamide gel electrophoresis differed between parent lines, but was not affected by the svs gene. A difference in the electrophoretic pattern for 27 kDa proteins was attributed to a new gene, Svp4 (J:9441).
References
Original: J:64453 Shukri N et al., "svs - seminal vesicle shape" Mouse News Lett 1988;81():56
All: 4 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/20/2009
MGI_4.31
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