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Gene Expression Data
Assay Details
Assay
Reference: 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
Assay type: RNA in situ
MGI Accession ID: MGI:5463583
Gene symbol: Larp7
Gene name: La ribonucleoprotein 7, transcriptional regulator
Probe: Larp7 probe
Probe preparation: Antisense labelled with digoxigenin RNA
Results
Specimen 2: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: embryo Present Ubiquitous 2A
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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05/07/2024
MGI 6.23 		The Jackson Laboratory