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Gene Expression Data
Assay Details
Assay
Reference: J:227879 Williamson KA, et al., Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. Am J Hum Genet. 2014 Feb 6;94(2):295-302
Assay type: Immunohistochemistry
MGI Accession ID: MGI:5763797
Gene symbol: Pax2
Gene name: paired box 2
Antibody: anti-Pax2 (#901001, #PRB-276P)
Detection system: Secondary antibody
Results
Specimen 2A: embryonic day 10.5 (more )
Note: Double labeled: red - Pax2; green - Yap1 (assay MGI:5763796).
Structure Level Pattern Image Note
TS17: eye Present 2A
Specimen 2B: embryonic day 10.5 (more )
Note: Double labeled: red - Pax2; green - Yap1 (assay MGI:5763796).
Structure Level Pattern Image Note
TS17: eye Present 2B
Specimen 2C: embryonic day 10.5 (more )
Note: Double labeled: red - Pax2; green - Yap1 (assay MGI:5763796).
Structure Level Pattern Image Note
TS17: eye Present 2C
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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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory