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Mapping Data
Experiment
  • Experiment
    TEXT-Physical Mapping
  • Chromosome
    2
  • Reference
    J:64907 Huang L, et al., The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency. Nat Genet. 1999 Nov;23(3):329-32
  • ID
    MGI:1891843
Genes
GeneAlleleAssay TypeDescription
Epb42
Bloc1s6 overlapping clones
D2Mit17
D2Mit30
D2Mit255
D2Mit396
D2Mit397
B2m
Notes
  • Experiment
    The authors used information from genetic mapping to estimate the Stx13bp1pa candidate region to be between Epb4.2 and B2m on Chromosome 2 in a 1 Mb interval. A YAC contig of the region was constructed using six overlapping YACs. YAC B4 (~530kb) carried the central portion of this interval. cDNA clones were identified using the YAC as a probe in a cDNA library. The authors were able to identify a cDNA showing reduced expression in pa mutant animals. Additional analysis revealed that mutations in this cDNA were responsible for the phenotype of Stx13bp1pa mutant mice. The gene has been given the symbol Stx13bp1pa (pallid).

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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