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sch Gene Detail
Summary
  • Symbol
    sch
  • Name
    scant hair
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98242
    NCBI Gene: 20258
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 9, Syntenic
  • Mapping Data
    7 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 in this gene stops hair growth.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-14311
References
more
  • Summaries
    All 9
    Phenotypes 1
  • Earliest
    J:8936 Bernstein SE, Hereditary hypotransferrinemia with hemosiderosis, a murine disorder resembling human atransferrinemia. J Lab Clin Med. 1987 Dec;110(6):690-705
  • Latest
    J:69953 Park YG, et al., Histological characteristics of the pelage skin of rough fur mice (C3H/HeJ- ruf/ruf). Exp Anim. 2001 Apr;50(2):179-82
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
04/30/2024
MGI 6.23 		The Jackson Laboratory