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Gene Expression Data
Assay Details
Assay
Reference: J:82084 Van de Putte T, et al., Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome. Am J Hum Genet. 2003 Feb;72(2):465-70
Assay type: RNA in situ
MGI Accession ID: MGI:7310106
Gene symbol: Cdh1
Gene name: cadherin 1
Results
Specimen 4E: embryonic day 8.5 (more )
Structure Level Pattern Image Note
TS13: surface ectoderm Present 4E
TS13: neural ectoderm Absent 4E Expression is turned off in neuroepithelium.

Specimen 4F: embryonic day 8.5; Zeb2tm1.2Yhi/Zeb2tm1.2Yhi (more )
Structure Level Pattern Image Note
TS13: neural ectoderm Present 4F Expression persisted in neural epithelium.


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
12/30/2025
MGI 6.24
The Jackson Laboratory