About   Help   FAQ
Frl Gene Detail
Summary
  • Symbol
    Frl
  • Name
    furloss
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:95579
    NCBI Gene: 103936
  • Alliance
    gene page
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    12 phenotypes from 3 alleles in 1 genetic background
    2 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mutations at this locus result in hair loss in the heterozygote and lethality of homozygotes in some alleles.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-9872
References
more
  • Summaries
    All 3
    Phenotypes 2
  • Earliest
    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
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory