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Mapping Data
Experiment
  • Experiment
    TEXT
  • Chromosome
    13
  • Reference
    J:90701 Ahituv N, et al., An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice. Mamm Genome. 2004 Jun;15(6):424-32
  • ID
    MGI:3580147
Genes
GeneAlleleAssay TypeDescription
Tfap2a
Notes
  • Experiment
    The Dorad mutation was mapped to an interval on mouse Chromosome 13 between D13Mit88 (21 cM) and D13Mit94 (31 cM) using 53 Dor+/- animals from a (C3HeB/FeJ-Dor x C57BL/6J)F1 x C3HeB/FeJ backcross. This region contains 8 candidate genes but Tcfap2a is theonly candidate gene with sequence variation between Dor mutants and wild type. An amino acid change (P59L) in the Tcfap2a coding sequence is found in Dor mutants. Furthermore, homozygous knockout Tcfap2atm1Will animals exhibit a phenotype similar to Dor mutants.

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
05/14/2024
MGI 6.23
The Jackson Laboratory