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Gene Expression Data
Assay Details
Assay
Reference: J:135966 Simpson MA, et al., Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development. Am J Hum Genet. 2007 Nov;81(5):906-12
Assay type: RNA in situ
MGI Accession ID: MGI:3795928
Gene symbol: Fam20c
Gene name: FAM20C, golgi associated secretory pathway kinase
Probe: FAM20C cDNA1
Probe preparation: Antisense labelled with S35 RNA
Visualized with: Autoradiography
Results
Specimen 3a: embryonic day 15.0 (more )
Structure Level Pattern Image Note
TS23: vertebral pre-cartilage condensation Present Regionally restricted 3a Strong expression within chondroblasts of somites and limb girdle.
TS23: limb mesenchyme Present Regionally restricted 3a Strong expression within chondroblasts of somites and limb girdle.
Specimen 3b: postnatal day 1 (more )
Structure Level Pattern Image Note
TS27: jaw Present Regionally restricted 3b In alveolar bone, expression in osteoblasts and ameloblasts, and strong expression in odontoblasts.
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
04/30/2024
MGI 6.23 		The Jackson Laboratory