Symbol Name ID

Yap1 yes-associated protein 1 MGI:103262

Reference

J:227879 Williamson KA, Rainger J, Floyd JA, Ansari M, Meynert A, Aldridge KV, Rainger JK, Anderson CA, Moore AT, Hurles ME, Clarke A, van Heyningen V, Verloes A, Taylor MS, Wilkie AO, Fitzpatrick DR, 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

Detailed expression data for these assays: 32 results

Indicates gene expression was analyzed but not necessarily detected.

Age	E9.5	E10.5	E11.5	E12.5	E	P
Immunohistochemistry (section)
In situ RNA (section)
Immunohistochemistry (whole mount)
In situ RNA (whole mount)
In situ reporter (knock in)
Northern blot
Western blot
RT-PCR
cDNA clones
RNase protection
Nuclease S1
Primer Extension

Comments: Optical projection tomography (OTP) was used to obtain the RNA in situ results.