RecName: Full=WW domain-binding protein 11; Short=WBP-11; AltName: Ful - Protein

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Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice. [Hum Mol Genet. 2020]
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Martin EMMA, Enriquez A, Sparrow DB, Humphreys DT, McInerney-Leo AM, Leo PJ, Duncan EL, Iyer KR, Greasby JA, Ip E, et al. Hum Mol Genet. 2020 Dec 4; 29(22):3662-3678.
Nucleocytoplasmic shuttling of the splicing factor SIPP1. [J Biol Chem. 2005]
Nucleocytoplasmic shuttling of the splicing factor SIPP1.
Llorian M, Beullens M, Lesage B, Nicolaescu E, Beke L, Landuyt W, Ortiz JM, Bollen M. J Biol Chem. 2005 Nov 18; 280(46):38862-9. Epub 2005 Sep 14.
WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: the proline glycine and methionine-rich motif. [Proc Natl Acad Sci U S A. 1998]
WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: the proline glycine and methionine-rich motif.
Bedford MT, Reed R, Leder P. Proc Natl Acad Sci U S A. 1998 Sep 1; 95(18):10602-7.

RefSeq protein isoforms
See 3 reference sequence protein isoforms for the Wbp11 gene.

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Transcript/Protein Information [PANTHER Classification System]
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Pseudoalteromonas shioyasakiensis strain LC2 12, whole genome shotgun sequence
Pseudoalteromonas shioyasakiensis strain LC2 12, whole genome shotgun sequence
gi|2519738928|ref|NZ_JASSPH01000001 gnl|WGS:NZ_JASSPH01|12

Nucleotide
NADH dehydrogenase subunit 4L (mitochondrion) [Myotis volans]
NADH dehydrogenase subunit 4L (mitochondrion) [Myotis volans]
gi|1277626283|ref|YP_009442763.1|

Protein
vitrin isoform 10 precursor [Homo sapiens]
vitrin isoform 10 precursor [Homo sapiens]
gi|1962008333|ref|NP_001378898.1|

Protein

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