About   Help   FAQ
thnh Gene Detail
Summary
  • Symbol
    thnh
  • Name
    thin hair
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:3798839
  • Alliance
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotypes from 1 allele in 1 genetic background
    2 images
    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
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
Homozygotes for this spontaneous mutation have sparse hair, abnormal hair follicle morphology, and folliculitis. Although all four hair types are present, fewer zigzag hairs are seen.
References
more
  • Summaries
    All 1
    Phenotypes 1
  • Earliest
    J:142872 Dionne L, et al., A new recessive hair mutation on Chromosome 9. MGI Direct Data Submission. 2009;

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 & Copyright Notice
Send questions and comments to User Support.
last database update
11/30/2021
MGI 6.17
The Jackson Laboratory