Symbol Name ID

Wbp11 WW domain binding protein 11 MGI:1891823

Reference

J:300837 Martin EMMA, Enriquez A, Sparrow DB, Humphreys DT, McInerney-Leo AM, Leo PJ, Duncan EL, Iyer KR, Greasby JA, Ip E, Giannoulatou E, Sheng D, Wohler E, Dimartino C, Amiel J, Capri Y, Lehalle D, Mory A, Wilnai Y, Lebenthal Y, Gharavi AG, Krzemien GG, Miklaszewska M, Steiner RD, Raggio C, Blank R, Baris Feldman H, Milo Rasouly H, Sobreira NLM, Jobling R, Gordon CT, Giampietro PF, Dunwoodie SL, Chapman G, Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. Hum Mol Genet. 2021 Jan 21;29(22):3662-3678

Detailed expression data for these assays: 15 results

Indicates gene expression was analyzed but not necessarily detected.

Age	E9.5	E10.5	E11.5	E12.5
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