ocd Gene Detail

Summary

• Symbol
  ocd
• Name
  osteochondrodystrophy

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:97399
  NCBI Gene: 18258
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr19:5808455-9910697 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 19, Syntenic
• Mapping Data
  15 experiments

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  12 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Find Mice (IMSR)
  1 strains or lines available

Mutations in this gene result in skeletal defects and male infertility.

Sequences &
Gene Models

• NCBI Gene
  18258

Other
Accession IDs

MGD-MRK-12971

References

• 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