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Mapping Data
Experiment
  • Experiment
    TEXT
  • Chromosome
    17
  • Reference
    J:92699 White RA, et al., Chromosomal localization, hematologic characterization, and iron metabolism of the hereditary erythroblastic anemia (hea) mutant mouse. Blood. 2004 Sep 1;104(5):1511-8
  • ID
    MGI:3581695
Genes
GeneAlleleAssay TypeDescription
Ttc7
D17Mit123
Pigf
Notes
  • Experiment
    The hea (hereditary erythroblastic anemia) locus was mapped using 100 homozygous mutant (hea/hea) animals from a (C57BL/6J-hea x MOLD/Rk)F1 x C57BL/6J-hea backcross. The hea phenotype showed linkage to approximately 55 cM on mouse Chromosome 17 near D17Mit123 (56.7 cM) and the Pigf gene (54.3 cM).

    The location of the hea mutation is in close proximity to the Ttc7fsn flaky skin mutation at 56.2 cM. Ttc7fsn mutants also exhibit erythropoiesis abnormalities similar to hea mutants. Complementation analysis was performed by crossing C57BL/6J-hea mutants to BALB/cByJ-Ttc7fsn mutants. Resulting progeny all exhibit an anemic phenotype. This finding is evidence that hea and Ttc7fsn are allelic and result from mutation within Ttc7.

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
12/10/2024
MGI 6.24
The Jackson Laboratory