about
P688
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlationIntronic polymorphisms within TFAP2B regulate transcriptional activity and affect adipocytokine gene expression in differentiated adipocytesTranscription factor AP-2 interacts with the SUMO-conjugating enzyme UBC9 and is sumolated in vivoThe role of Sp1 and AP-2 in basal and protein kinase A--induced expression of mitochondrial serine:pyruvate aminotransferase in hepatocytesGenetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitusComparative expression profiling identifies an in vivo target gene signature with TFAP2B as a mediator of the survival function of PAX3/FKHRCloning and characterization of a second AP-2 transcription factor: AP-2 betaThe transcription factor TFAP2B is associated with insulin resistance and adiposity in healthy adolescentsTranscription factor AP-2 regulates human insulin-like growth factor binding protein-5 gene expressionAP2 transcription factor induces apoptosis in retinoblastoma cells
P921
Q24291566-082A335D-6158-4C3E-88D5-C580DEB332E8Q24299630-170DD730-D0B9-43DD-8A4E-7299279CABD7Q24299957-F65DAE66-6F12-430A-B587-FB39BF4712F8Q24304141-038B678D-F717-4E05-B94A-C47BA53E408BQ24304627-82F0D2AE-A12F-411C-A698-A33A72D279B1Q24306915-F7866B2B-3D70-4A69-9FF6-ABF6D86B97EBQ24309166-4916C854-9A37-4253-B5D7-DCF05B1F3301Q24310267-D16073B1-92CD-4CD6-8371-835AC4A1D65AQ24310632-B0CB5735-5DE6-41F3-9AC8-1277D2F1E0DCQ24337909-15A18A73-D075-4C3E-A61B-2F502446C24E
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Transcription factor AP-2 beta
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Transcription factor AP-2 beta
@en
type
label
Transcription factor AP-2 beta
@en
altLabel
AP2-beta
@en
Activating enhancer-binding protein 2-beta
@en
TFAP2B
@en
activating enhancer binding protein 2 beta
@en
transcription factor AP-2-beta
@en
prefLabel
Transcription factor AP-2 beta
@en
P637
P680
P681
P682
P352
P279
P31
P352
P637
XP_011513139
XP_016866722
XP_016866723
XP_016866724
P680
P682
P702
P703
P705
ENSP00000342252
ENSP00000377265