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ocd Gene Detail
Summary
  • Symbol
    ocd
  • Name
    osteochondrodystrophy
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:97399
    NCBI Gene: 18258
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr19:5808455-9910697 bp
    From MGI annotation of GRCm39
  • View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 19, Syntenic
  • Mapping Data
    15 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    12 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
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.
Mutations in this gene result in skeletal defects and male infertility.
Sequences &
Gene Models
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Other
Accession IDs
less
MGD-MRK-12971
References
more
  • Summaries
    All 4
    Phenotypes 1
  • Earliest
    J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4
  • Latest
    J:47269 Poirier C, et al., A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region. Mamm Genome. 1998 May;9(5):390-1

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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last database update
08/03/2022
MGI 6.21
The Jackson Laboratory