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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    19
  • Reference
    J:23584 Cook SA, et al., Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration. Mamm Genome. 1995 Mar;6(3):187-91
  • ID
    MGI:44713
Genes
GeneAlleleAssay TypeDescription
Ighmbp2 visible phenotype
D19Sel2 reported elsewhere
Pygm reported elsewhere
Cntf reported elsewhere
Pomc-ps1 reported elsewhere
D19Mit1 reported elsewhere
Cyp2c29 reported elsewhere
Got1 reported elsewhere
Notes
  • Reference
    Data submitted in MGD under accession number MGD-CREX-162.
  • Experiment
    Authors map nmd to Chromosome 19 using an intersubspecific intercross between (CAST/Ei x B6.Bks-nmd2J/+)F1 x (CAST/Ei x B6.Bks-nmd2J/+)F1. Only homozygous nmd mutants were scored for mapping (N = 138 meiosis). Recombination distance was reported as follows: nmd - 1.45 +/- 1.02 cM - D19Sel2 - Pygm - 5.64 +/- 2.07 cM - Cntf - 0.89 +/- 0.89 cM - Pomc2 - 0.85 +/- 0.84 cM - D19Mit16 - 12.71 +/- 3.07 cM - Cyp2c - 3.39 +/- 1.67 cM - Got1.

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
10/29/2024
MGI 6.24
The Jackson Laboratory