Minth Other Genome Feature Detail

Summary

• Symbol
  Minth
• Name
  Moloney MuLV integration site, EC cells, h

• Feature Type
  unclassified other genome feature
• IDs
  MGI:96989
  NCBI Gene: 108503

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome Unknown

Mutations,
Alleles, and
Phenotypes

The Mint viral integration sites allow expression of proviral sequences in murine embryonal carcinoma cells, which do not normally express retroviruses. Proviral expression is caused by cellular enhancer or promoter sequences flanking the proviral integration site.

Sequences &
Gene Models

• NCBI Gene
  108503

Other
Accession IDs

MGD-MRK-12239

References

• Summaries
  All 2
• Earliest
  J:2070 Taketo M, et al., Mapping of recombinant retrovirus integration sites that cause expression of the viral genome in murine embryonal carcinoma cells. Mamm Genome. 1992;2(4):240-5