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Gene Expression Data
Assay Details
Assay
Reference: J:43842 Quaderi NA, et al., Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nat Genet. 1997 Nov;17(3):285-91
Assay type: RNA in situ
MGI Accession ID: MGI:7276254
Gene symbol: Mid1
Gene name: midline 1
Probe: ME10.2
Probe preparation: Antisense labelled with digoxigenin RNA
Results
Specimen 5a: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: 1st branchial arch mandibular component Strong 5a Expression is along the proximo-distal axis of the arches.
TS17: 1st branchial arch maxillary component Strong 5a Expression is along the proximo-distal axis of the arches.
TS17: 2nd branchial arch Strong 5a Expression is along the proximo-distal axis of the arches.
TS17: embryo Present Ubiquitous 5a
Specimen 5b: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: branchial arch Strong Regionally restricted 5b Expression is along the proximo-distal axis of the arches.
Specimen 5c: embryonic day 10.5 (more )
Structure Level Pattern Image Note
TS17: branchial arch Strong Regionally restricted 5c Expression is along the medio-lateral axis of the arches.
TS17: heart Absent 5c
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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03/25/2025
MGI 6.24 		The Jackson Laboratory