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endoglin probe1 Probe Detail
Nucleotide
Probe/Clone
  • Name
    endoglin probe1
  • Sequence Type
    Not Specified
  • ID
    MGI:6109973
Source
  • Species
    Not Specified
Genes
Eng endoglin
Expression
  • Assay Results
    2
References
J:158706 Meyer E, et al., Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome). Am J Hum Genet. 2010 Mar 12;86(3):471-8
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
05/21/2024
MGI 6.23 		The Jackson Laboratory