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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:7310090
Gene symbol: Twist1
Gene name: twist basic helix-loop-helix transcription factor 1
Results
Specimen 2A: embryonic day 8.5 (more )
Structure Level Pattern Image Note
TS13: head mesenchyme Present 2A
TS13: 1st branchial arch mesenchyme derived from neural crest Present 2A
Specimen 2B: embryonic day 8.5; Zeb2tm1.2Yhi/Zeb2tm1.2Yhi (more )
Structure Level Pattern Image Note
TS13: 1st branchial arch Absent 2B Reduced expression in head mesenchyme
TS13: head mesenchyme Absent 2B Reduced expression in head mesenchyme
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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Funding Information
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03/25/2025
MGI 6.24 		The Jackson Laboratory