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us Gene Detail
Summary
  • Symbol
    us
  • Name
    urogenital syndrome
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98918
    NCBI Gene: 22277
  • Alliance
Location &
Maps
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  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome 2, Syntenic
  • Mapping Data
    5 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    24 phenotypes from 1 allele in 1 genetic background
    2 phenotype references
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.
Homozygous mutants have abnormal axial skeleton and urogenital organs. Mutants show reduced viability, retarded growth, thin hair coat, head-shaking, and serious defects of kidney, skeleton and reproductive organs.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-15375
References
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  • Summaries
    All 4
    Phenotypes 2
  • Earliest
    J:14466 Lane PW, et al., Urogenital syndrome (us): a developmental mutation on chromosome 2 of the mouse. Mamm Genome. 1993 Sep;4(9):481-4

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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last database update
11/16/2021
MGI 6.17
The Jackson Laboratory