About   Help   FAQ
Larp7 probe Probe Detail
Nucleotide
Probe/Clone
  • Name
    Larp7 probe
  • Sequence Type
    cDNA
  • ID
    MGI:5463586
  • Note
    The authors used a combination of two non-overlapping probes (MGI:5463575 and MGI:5463578) for the assay.
Source
  • Species
    mouse, laboratory
  • Age
    postnatal adult
  • Tissue
    liver
Genes
Larp7 La ribonucleoprotein 7, transcriptional regulator
Expression
  • Assay Results
    1
References
J:190574 Alazami AM, et al., Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism. Hum Mutat. 2012 Oct;33(10):1429-34
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
05/21/2024
MGI 6.23 		The Jackson Laboratory