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ME10.2 Probe Detail
Nucleotide
Probe/Clone
  • Name
    ME10.2
  • Sequence Type
    cDNA
  • ID
    MGI:1203968
  • Insert Size
    ~1.5kb
Source
  • Species
    mouse, laboratory
  • Age
    embryonic day 11.5
  • Tissue
    embryo
Genes
Mid1 midline 1
Expression
  • Assay Results
    7
Sequences
Y14848 (GenBank | EMBL | ENA | DDBJ | MGI Sequence Detail)
Polymorphisms
J:46361 Dal Zotto L, et al., Hum Mol Genet. 1998 Mar;7(3):489-99
Endonuclease Gene Allele Fragments Strains
PstI Mid1 b 2.8kb C57BL/6JEiJ
c 2.0, 2.5kb C57BL/10
s 13.0kb SKIVE
PvuII Mid1 b not given C57BL/6JEiJ
s not given SPRET/EiJ
References
J:43842 Quaderi NA, et al., Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nat Genet. 1997 Nov;17(3):285-91
J:46361 Dal Zotto L, et al., The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Hum Mol Genet. 1998 Mar;7(3):489-99
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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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory