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Xlhl Gene Detail
Summary
  • Symbol
    Xlhl
  • Name
    X-linked hair loss
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:5585402
  • Alliance
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome X, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 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.
Male mice hemizygous for a spontaneous allele exhibit sparse hair and abnormal hair follicle morphology. Heterozygous mutant females show focal hair loss and abnormal hair follicle morphology while homozygous mutant females are nearly as bald as hemizygous males.
References
more
  • Summaries
    All 1
    Phenotypes 1
  • Earliest
    J:213765 Karst SY, et al., X-linked hair loss, a spontaneous mutation similar to bad hair day. MGI Direct Data Submission. 2014;

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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Funding Information
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory