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Gene Expression Data
Assay Details
Assay
Reference: J:308706 Lui JC, et al., QRICH1 mutations cause a chondrodysplasia with developmental delay. Clin Genet. 2019 Jan;95(1):160-164
Assay type: RNA in situ
MGI Accession ID: MGI:6831043
Gene symbol: Qrich1
Gene name: glutamine-rich 1
Probe: Qrich1 cDNA
Probe preparation: Antisense labelled with digoxigenin RNA
Visualized with: Alkaline phosphatase
Results
Specimen S2C: embryonic day 12.5 (more )
Structure Level Pattern Image Note
TS20: neocortex Present Regionally restricted S2C Expressed in the prefrontal cortex.
TS20: limb Present S2C
TS20: mandibular process Present S2C
TS20: maxillary process Present S2C


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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory