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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:7310089
Gene symbol: Zeb2
Gene name: zinc finger E-box binding homeobox 2
Results
Specimen 1B: embryonic day 8.5 (more )
Structure Level Pattern Image Note
TS13: neural plate Present Regionally restricted 1B Expression in neuroepithelium where expression levels closely follow maturation of neural plate.
TS13: rhombomere 3 Absent 1B
TS13: rhombomere 5 Absent 1B
Specimen 1C: embryonic day 8.5 (more )
Structure Level Pattern Image Note
TS13: neural plate Present Regionally restricted 1C
TS13: rhombomere 3 Absent 1C
TS13: rhombomere 5 Absent 1C
TS13: neural crest Strong Regionally restricted 1C High level of expression in premigratory neural crest cells of cranial and postotic vagal origin.
Specimen 1D: embryonic day 8.5 (more )
Structure Level Pattern Image Note
TS13: neural plate Present Regionally restricted 1D Expression in neuroepithelium.
TS13: migrating neural crest Present Regionally restricted 1D Expression in migrating neural crest cells of cranial origin.
TS13: branchial arch mesenchyme Present 1D
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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01/06/2026
MGI 6.24 		The Jackson Laboratory