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Diap1 cDNA2 Probe Detail
Nucleotide
Probe/Clone
  • Name
    Diap1 cDNA2
  • Sequence Type
    cDNA
  • ID
    MGI:5812112
  • Region Covered
    nucleotides 3062-3861 of NM_007858
  • Insert Size
    0.799kb
Source
  • Species
    mouse, laboratory
Genes
Diaph1 diaphanous related formin 1
Expression
  • Assay Results
    34
References
J:228552 Ercan-Sencicek AG, et al., Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. Eur J Hum Genet. 2015 Feb;23(2):165-72
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
05/07/2024
MGI 6.23 		The Jackson Laboratory