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ba Gene Detail
Summary
  • Symbol
    ba
  • Name
    bare
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88128
    NCBI Gene: 12011
  • Alliance
    gene page
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    19 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.
Mice homozygous for this allele display growth retardation and abnormal hair development and are strikingly hairless by 6 months of age.
Sequences &
Gene Models
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Other
Accession IDs
less
MGD-MRK-1493
References
more
  • Summaries
    All 3
    Phenotypes 1
  • Earliest
    J:291 Randelia HP, et al., "Bare", a new hairless mutant in the mouse - genetics and histology. Genet Res. 1961;2(2):283-89
  • Latest
    J:7208 Andrews SJ, et al., Linkage analyses and biochemical genetics of sorbitol dehydrogenase-1 (Sdh-1) in the mouse. Biochem Genet. 1983 Aug;21(7-8):809-17
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
11/12/2024
MGI 6.24 		The Jackson Laboratory