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Gene Expression Data
Assay Details
Assay
Reference: J:146769 Choi M, et al., Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse. PLoS Genet. 2009 Feb;5(2):e1000395
Assay type: RNA in situ
MGI Accession ID: MGI:3841658
Gene symbol: Tbx1
Gene name: T-box 1
Results
Specimen 4A: embryonic day 8.0 (more )
Structure Level Pattern Image Note
TS12: foregut diverticulum Present 4A Expression in the pharyngeal area.

Specimen 4B: embryonic day 8.0; Chrdtm1Emdr/Chrdtm1Emdr, Tbx1m1Jlk/Tbx1m1Jlk (more )
Structure Level Pattern Image Note
TS12: foregut diverticulum Weak Regionally restricted 4B Authors report reduced expression in pharyngeal area of homozygotes with a DGS-like phenotype.

Specimen 4C: embryonic day 8.0 (more )
Structure Level Pattern Image Note
TS12: foregut diverticulum Present Regionally restricted 4C Expression in the pharyngeal area.

Specimen 4D: embryonic day 8.0; Chrdtm1Emdr/Chrdtm1Emdr, Tbx1m1Jlk/Tbx1m1Jlk (more )
Structure Level Pattern Image Note
TS12: foregut diverticulum Weak Regionally restricted 4D Authors report reduced expression in pharyngeal area of homozygotes with a DGS-like phenotype.


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
05/14/2024
MGI 6.23
The Jackson Laboratory