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Frlb
Radiation induced Allele Detail
Summary
Symbol: Frlb
Name: furloss; furloss b
MGI ID: MGI:1856033
Gene: Frl  Location: unknown  
Alliance: Frlb page
Mutation
origin
Strain of Origin:  (101 x C3H)F1
Mutation
description
Allele Type:    Radiation induced
Inheritance:    Dominant
Phenotypes
Key:
hm homozygous ht heterozygous tg involves transgenes phenotype observed
cn conditional genotype  cx complex: > 1 genome feature ot other: hemizygous, indeterminate,... N normal phenotype
Genotype/
Background:
Allelic Composition
Genetic Background
Cell Line(s)
Not Specified
 
Frlb/Frl+
Not Specified
 
Phenotypes:
Affected Systems
show or hide all annotated terms
   
growth/size/body
decreased birth body size
decreased body weight
integument
abnormal coat appearance
abnormal hair growth
focal hair loss
progressive hair loss
sparse hair
striated fur
abnormal hair shedding
wrinkled skin
mortality/aging
decreased survivor rate
prenatal lethality, incomplete penetrance
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Frl Mutation:  4 strains or lines available
References
Original:  J:7103 Stelzner KF, Four dominant autosomal mutations affecting skin and hair development in the mouse. J Hered. 1983 May-Jun;74(3):193-6
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
12/10/2024
MGI 6.24
The Jackson Laboratory