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thf Gene Detail
Summary
  • Symbol
    thf
  • Name
    thin fur
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98741
    NCBI Gene: 21831
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 17, Syntenic
  • Mapping Data
    13 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    5 phenotypes from 1 allele in 1 genetic background
    1 phenotype reference
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 cause abnormal hair development.
Sequences &
Gene Models
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Other
Accession IDs
less
MGD-MRK-15090
References
more
  • Summaries
    All 8
    Phenotypes 1
  • Earliest
    J:5276 Key M, et al., Thin fur, a recessive mutant on chromosome 17 of the mouse. J Hered. 1972 Mar-Apr;63(2):97-8
  • Latest
    J:221436 Liu W, et al., Activation of NF-kappaB signaling pathway in HSV-1-induced mouse facial palsy: Possible relation to therapeutic effect of glucocorticoids. Neuroscience. 2015 Mar 19;289:251-61
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
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory