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Krt71Ca
Spontaneous Allele Detail

Nomenclature
Symbol: Krt71Ca
Name: keratin 71; caracul
MGI ID: MGI:1855990
Synonyms: Ca
Gene: Krt71   Location: Chr15:101564381-101573540 bp, - strand    Genetic Position: Chr15, 63.2 cM
Mutation
origin
Strain of Origin: Swiss stock
Mutation
description
Allele Type: Spontaneous
Mutation: Single point mutation
  Sequence analysis of Krt2-6g identified the transversion of an adenosine to a cytosine at nucleotide 1292, resulting in an alanine to aspartic acid missense mutation at codon 431 (A431D).
Inheritance: Dominant
Find Mice (IMSR) Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Krt71 Mutation: 7 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
 
cx3
  
skin/coat/nails          
  
touch/vibrissae          
 
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 hm1   
Krt71Ca/Krt71Ca Not Specified
  
 ht2   
Krt71Ca/Krt71+ Not Specified
  
 cx3   
Hag/Hag+
Krt71Ca/Krt71+
involves: C3H/HeN * C57BL/6ByJ
References
Original: J:13054 Dunn LC, "Caracul, a dominant mutation." J Hered 1937;28():334
All: 5 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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