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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: RT-PCR
MGI Accession ID: MGI:5763784
Gene symbol: Yap1
Gene name: yes-associated protein 1
Probe: m3 set
Results Image: 1I m3
 Sample Information Bands Other Sample Information
Lane AgeStructure Size Not Specified Amount Genetic BackgroundMutant Allele(s)Sex
Kidney P adult TS28: metanephros Present Not Specified Not Specified Not Specified
Brain P adult TS28: brain Present Not Specified Not Specified Not Specified
Eye P adult TS28: eye Present Not Specified Not Specified Not Specified
Kidney Tissue age not specified: no data stored
Brain Tissue age not specified: no data stored
Eye Tissue age not specified: no data stored
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
05/07/2024
MGI 6.23 		The Jackson Laboratory