Hma Gene Detail

Summary

• Symbol
  Hma
• Name
  HPRT mobility alteration

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:96111
  NCBI Gene: 109940
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 7, Syntenic
• Mapping Data
  7 experiments

Mutations,
Alleles, and
Phenotypes

This locus controls HPRT electrophoretic variation in erythrocytes. The dominant a allele is seen in A/J, DBA/2J and CBA/J; the b allele in C57BL/6J, SJL/J and LT/Sv. Strain distribution is the same as Hbb alleles d and s, suggesting HPRT mobility variation may be an effect of HBB chain difference.

Sequences &
Gene Models

• NCBI Gene
  109940

Other
Accession IDs

MGD-MRK-10745

References

• Summaries
  All 4
• Earliest
  J:6291 Nesbitt MN, et al., Isoenzyme pattern of HPRT in murine erythrocytes: control by an autosomal locus. Biochem Genet. 1979 Oct;17(9-10):957-64
• Latest
  J:48897 Ben-Zur T, et al., Mapping homologs of Drosophila odd Oz (odz): Doc4/Odz4 to mouse chromosome 7, Odz1 to mouse chromosome 11; and ODZ3 to human chromosome Xq25. Genomics. 1999 May 15;58(1):102-3