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Slc27a4wrfr
Spontaneous Allele Detail

Nomenclature
Symbol: Slc27a4wrfr
Name: solute carrier family 27 (fatty acid transporter), member 4; wrinkle free
MGI ID: MGI:2445864
Gene: Slc27a4   Location: Chr2:29658154-29673042 bp, + strand    Genetic Position: Chr2, 19.0 cM, cytoband B
Histological analysis of the Slc27a4wrfr/Slc27a4wrfr mouse

Show the 2 image(s) involving this allele.

Mutation
origin
Strain of Origin: (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type: Spontaneous
Mutation: Transposon insertion
  This mutation is an insertion of a B2-type murine retrotransposon into the third exon of the gene. Northern analysis failed to detect mRNA for this gene in mutant mice. (J:83282)
Inheritance: Recessive
Find Mice (IMSR) Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Slc27a4 Mutation: 2 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
  
behavior/neurological          
  
digestive/alimentary system          
  
lethality/prenatal-perinatal          
  
respiratory system          
  
skin/coat/nails          
 
  
Disease Models          
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 hm1   Disease Model  images  
Slc27a4wrfr/Slc27a4wrfr involves: 129 * C57BL/6J
Disease
models
Mouse Models
of Human Disease
NoteGenotypeRef(s)
 
Allelic Composition
Genetic Background
Models with phenotypic similarity to human diseases not associated with human SLC27A4.
Tight Skin Contracture Syndrome, Lethal
OMIM ID: 275210
 
 
hm1
Slc27a4wrfr/Slc27a4wrfrinvolves: 129 * C57BL/6JJ:83282
References
Original: J:83282 Moulson CL et al., "Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development." Proc Natl Acad Sci U S A 2003 Apr 29;100(9):5274-9
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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