Gene Expression Literature Summary

• Symbol: Wbp11
• Name: WW domain binding protein 11
• ID: MGI:1891823

2 matching records from 2 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.

Age	E7.5	E9.5	E10.5	E11.5	E12.5
Immunohistochemistry (section)			1	1	1
Immunohistochemistry (whole mount)		1
Western blot		1
RT-PCR	1		1
cDNA clones	1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available

Wbp11  WW domain binding protein 11   (Synonyms: 2510026P17Rik, D6Wsu113e, Npwbp, SIPP1)
Results	Reference
2*	J:50869 Ko MSH, Threat TA, Wang X, Horton JH, Cui Y, Pryor E, Paris J , Wells-Smith J , Kitchen JR , Rowe LB , Eppig J , Satoh T , Brant L , Fujiwara H , Yotsumoto S , Nakashima H, Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome. Hum Mol Genet. 1998 Nov;7(12):1967-78
6*	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