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Gene Expression Data
Assay Details
Assay
Reference: J:187427 Rainger J, et al., Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. Hum Mol Genet. 2012 Sep 15;21(18):3969-83
Assay type: RNA in situ
MGI Accession ID: MGI:5441728
Gene symbol: Cad
Gene name: carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase
Probe: Cad probe
Probe preparation: Antisense labelled with digoxigenin DNA
Assay notes: The data is from optical projection tomography.
Results
Specimen Left: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: surface ectoderm Present Regionally restricted 5_Cad whole-mount Expression was seen throughout the surface of the embryo.
TS17: 1st branchial arch mandibular component Strong 5_Cad whole-mount
TS17: 1st branchial arch maxillary component Strong 5_Cad whole-mount
TS17: 2nd branchial arch Strong 5_Cad whole-mount
TS17: forelimb bud Strong 5_Cad whole-mount
TS17: hindlimb bud Strong 5_Cad whole-mount
TS17: somite Strong 5_Cad whole-mount
Specimen Middle: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: 1st branchial arch Strong 5_Cad transverse
TS17: 2nd branchial arch Strong 5_Cad transverse
TS17: surface ectoderm Present Regionally restricted 5_Cad transverse Expression was seen throughout the surface of the embryo.
Specimen Right: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: forelimb bud Strong 5_Cad coronal
TS17: surface ectoderm Present Regionally restricted 5_Cad coronal Expression was seen throughout the surface of the embryo.
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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04/16/2024
MGI 6.23 		The Jackson Laboratory