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Gene Expression Data
Assay Details
Assay
Reference: J:191406 Laue K, et al., Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid. Am J Hum Genet. 2011 Nov 11;89(5):595-606
Assay type: RNA in situ
MGI Accession ID: MGI:5911757
Gene symbol: Cyp26b1
Gene name: cytochrome P450, family 26, subfamily b, polypeptide 1
Probe: Cyp26b1 cDNA5
Probe preparation: Antisense RNA
Results
Specimen 2C: embryonic day 15.0 (more )
Structure Level Pattern Image Note
TS23: forelimb interphalangeal joint Present 2C Cyp26b1
TS23: forelimb digit Present Regionally restricted 2C Cyp26b1 Expression is close to developing tendons at the distal ends of phalangeal primordia.
Specimen S5a: postnatal day 0 (more )
Structure Level Pattern Image Note
TS27: coronal suture Present Single cells S5a Expression is around the calvarial tips.
TS27: chondrocranium Present Single cells S5a Expression is in cells lining the calvarial plates or embedded within the calvarial bone.
Specimen S5c: postnatal day 0 (more )
Structure Level Pattern Image Note
TS27: chondrocranium Present Single cells S5c Expression is in cells embedded within the calvarial bone.
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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03/25/2025
MGI 6.24 		The Jackson Laboratory