Minta Other Genome Feature Detail

Summary

• Symbol
  Minta
• Name
  Moloney MuLV integration site, EC cells, a

• Feature Type
  unclassified other genome feature
• IDs
  MGI:96983
  NCBI Gene: 111674

Location &
Maps

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

• Genetic Map
  Chromosome 10, Syntenic
• Mapping Data
  9 experiments

Strain
Comparison

• RFLP
  5

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
  111674

Molecular
Reagents

• All nucleic 2

  Genomic 1

  Other 1

Other
Accession IDs

MGD-MRK-12233

References

• Summaries
  All 10
• Earliest
  J:1142 Apte SS, et al., Cloning of the human and mouse type X collagen genes and mapping of the mouse type X collagen gene to chromosome 10. Eur J Biochem. 1992 May 15;206(1):217-24
• Latest
  J:64475 Puttagunta R, et al., Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints. Genome Res. 2000 Sep;10(9):1369-80