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Mapping Data
Experiment
  • Experiment
    TEXT
  • Chromosome
    2
  • Reference
    J:49062 Williamson CM, et al., Localisation of the imprinted gene neuronatin, Nnat, confirms and refines the location of a second imprinting region on mouse chromosome 2. Cytogenet Cell Genet. 1998;81(1):73-8
  • ID
    MGI:1277803
Genes
GeneAlleleAssay TypeDescription
T(2;8)26H visible phenotype
Nnat PCR amplified length variant Nnat-pA1, Nnat-pB1
T(2;4)1Sn visible phenotype
T(2;4)1Go visible phenotype
Notes
  • Experiment
    Nnat was positioned relative to several translocation breakpoints on mouse Chromosome 2 by the analysis of the expression of Nnat maternal or paternal alleles in mice that have duplications/deficiencies revelant autosomal regions. Nnat lies proximal of the Chromosome 2 breakpoints in T(2;4)1Go and T(2;4)1Sn and between the Chromosome 2 breakpoints in T(2;8)26H and T(2;4)1Sn. As a result of the expression studies Nnat is assigned to band H1 on mouse Chromosome 2.

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