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Mapping Data
Experiment
  • Experiment
    TEXT-Physical Mapping
  • Chromosome
    14
  • Reference
    J:87686 Burgess RW, et al., Evidence for a conserved function in synapse formation reveals Phr1 as a candidate gene for respiratory failure in newborn mice. Mol Cell Biol. 2004 Feb;24(3):1096-105
  • ID
    MGI:3028769
Genes
GeneAlleleAssay TypeDescription
Mycbp2 Deletion Mapping
Scel Deletion Mapping
D14J6 Deletion Mapping
D14J13 Deletion Mapping
Notes
  • Experiment
    The positions of the Phr1, Scel, and TC255155 (novel Gene) transcripts based on alignments with the genomic sequence are shown to be within the 48Uthc and 9thW deletion chromosomes. Markers D14J6 and D14J13 mark the proximal and distal boundries of the 480 kb respiratory distrss critical region of mouse Chromosome 14 which is within the 9thW deletion. 9thW includes both Phr1 and Scel ( opposite transcription). The authors suggest that the loss of Phr1 expression correlates with the respiratory distress phenotype.

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
04/23/2024
MGI 6.23
The Jackson Laboratory