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DN10 Probe Detail
Nucleotide
Probe/Clone
  • Name
    DN10
  • Sequence Type
    cDNA
  • ID
    MGI:10882
  • Insert Size
    3.2kb
Source
  • Species
    human
  • Age
    embryonic
  • Tissue
    brain
Genes
Oca2 oculocutaneous albinism II
Polymorphisms
J:14250 Nicholls RD, Mouse News Lett. 1989;84:87-88
Endonuclease Gene Allele Fragments Strains
MspI Oca2 a not given AKR, C3H/HeJ
b not given C57BL/6J, C57L/J
c not given SJL/J
d not given DBA/2J
J:3600 Rinchik EM, et al., Nature. 1993 Jan 7;361(6407):72-6
Endonuclease Gene Allele Fragments Strains
BamHI Oca2 r 6.0,3.3kb 129/Rl-Oca2p Tyrc-ch
s 7.7,3.6kb M. spretus
References
J:14250 Nicholls RD, A cDNA from proximal human Chromosome 15q maps near Mtv-1 on mouse Chromosome 7. Mouse News Lett. 1989;84:87-88
J:11587 Chaillet JR, et al., The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7. Genomics. 1991 Nov;11(3):773-6
J:3600 Rinchik EM, et al., A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism. Nature. 1993 Jan 7;361(6407):72-6
J:4101 Nicholls RD, et al., Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4

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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory