NR2E3 and MYBBP1A

Data Source:
HPRD (in vivo)

		NR2E3	MYBBP1A
Description		nuclear receptor subfamily 2 group E member 3	MYB binding protein 1a
Image			No pdb structure
GO Annotations	Cellular Component	Nucleus Nucleoplasm Transcription Regulator Complex	Nucleus Nucleoplasm Nucleolus Cytoplasm Membrane NLS-dependent Protein Nuclear Import Complex Intracellular Membrane-bounded Organelle
	Molecular Function	RNA Polymerase II Cis-regulatory Region Sequence-specific DNA Binding DNA-binding Transcription Activator Activity, RNA Polymerase II-specific Steroid Hormone Receptor Activity Nuclear Receptor Activity Protein Binding Zinc Ion Binding Sequence-specific DNA Binding	Transcription Corepressor Activity RNA Binding Transcription Factor Binding Sequence-specific DNA Binding E-box Binding
	Biological Process	Negative Regulation Of Transcription By RNA Polymerase II Regulation Of Transcription By RNA Polymerase II Transcription Initiation From RNA Polymerase II Promoter Signal Transduction Visual Perception Phototransduction Negative Regulation Of Cell Population Proliferation Cell Differentiation Intracellular Receptor Signaling Pathway Eye Photoreceptor Cell Development Steroid Hormone Mediated Signaling Pathway Positive Regulation Of Transcription By RNA Polymerase II Anatomical Structure Development Retina Development In Camera-type Eye	Osteoblast Differentiation Regulation Of Transcription, DNA-templated Respiratory Electron Transport Chain Circadian Regulation Of Gene Expression Cellular Response To Glucose Starvation Ribosome Biogenesis Positive Regulation Of Gene Expression, Epigenetic Negative Regulation Of Transcription, DNA-templated Positive Regulation Of Cell Cycle Arrest Intrinsic Apoptotic Signaling Pathway By P53 Class Mediator Positive Regulation Of Anoikis
Pathways			B-WICH complex positively regulates rRNA expression
Drugs
Diseases		Vitreoretinal degeneration, including: Stickler syndrome type I (STL1); Stickler syndrome type II (STL2); Snowflake vitreoretinal degeneration (SVD); Wagner syndrome 1 (WGN1); Knobloch syndrome (KNO); Enhanced S-cone syndrome (ESCS); Autosomal dominant vitreoretinochoroidopathy (ADVIRC) Retinitis pigmentosa (RP)
GWAS		Hematocrit ( 32888494) Hemoglobin ( 32888494) Macular thickness ( 30535121) Metabolite levels (HVA/MHPG ratio) ( 23319000) Red blood cell count ( 32888494)
Interacting Genes		29 interacting genes: BCL11A CDK9 CRX DEDD2 DHX30 ELAVL2 HDAC1 HDAC3 HOXC13 IRF9 MYBBP1A NCOR1 NR1D1 NR3C1 NRL POLR3D PPARG RARA RBBP4 RBBP7 RBFOX2 RBL1 RXRA RXRB SIN3A SNAPC1 TBL3 WDR5 ZNF232	14 interacting genes: APP AR DHX30 DUX4 ESR1 HOXB9 JUN MYB NR2E3 PCNA PPARGC1A PTEN TP53 UBE2I
Entrez ID		10002	10514
HPRD ID		05132	05349
Ensembl ID		ENSG00000278570	ENSG00000132382
Uniprot IDs		F1D8Q9 Q9Y5X4	Q9BQG0
PDB IDs		4LOG
Enriched GO Terms of Interacting Partners?
Tagcloud ?
Tagcloud (Difference) ?
Tagcloud (Intersection) ?