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oar Gene Detail
Summary
  • Symbol
    oar
  • Name
    oarleg
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:3850107
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Chr5:120018497-125528566 bp
    From MGI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 5, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 phenotypes from 1 allele in 1 genetic background
    1 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
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.
When lifted by the tail, homozygotes point their toes straight out and hold their limbs stiffly and when both hindlimbs are affected it results in a stiff gait.
References
more
  • Summaries
    All 1
    Phenotypes 1
  • Earliest
    J:152522 Harris BS, et al., Oarleg: A new autosomal recessive mutation is mapped to Chromosome 5. 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
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory