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Gene Expression Data
Assay Details
Assay
Reference: J:322658 Calpena E, et al., Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders. J Med Genet. 2022 Feb;59(2):165-169
Assay type: In situ reporter (knock in)
MGI Accession ID: MGI:7261174
Gene symbol: Six1
Gene name: sine oculis-related homeobox 1
Reporter: lacZ
Direct Detection
Results
Specimen 1E: embryonic day 18.5; Six1tm1Mair/Six1+ (more )
Structure Level Pattern Image Note
TS26: brain dura mater Present Regionally restricted 1E Expression in a layer basal to growing bones, likely corresponding to dura mater.
TS26: parietal bone Absent 1E No significant expression in osteogenic fronts.

Specimen 1F: embryonic day 18.5; Six1tm1Mair/Six1+ (more )
Structure Level Pattern Image Note
TS26: sagittal suture Present Regionally restricted 1F Expression extending into mesenchyme of future sagital suture.

Specimen S2B: embryonic day 18.5; Six1tm1Mair/Six1+ (more )
Structure Level Pattern Image Note
TS26: frontal bone Absent S2B No significant expression in osteogenic fronts.

Specimen S2C: embryonic day 18.5; Six1tm1Mair/Six1+ (more )
Structure Level Pattern Image Note
TS26: coronal suture Absent S2C No significant expression mid-sutural mesenchyme of coronal sutures


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
03/25/2025
MGI 6.24
The Jackson Laboratory