MYBBP1A and NR2E3

Data Source:
HPRD (in vivo)

		MYBBP1A	NR2E3
Description		MYB binding protein 1a	nuclear receptor subfamily 2 group E member 3
Image		No pdb structure
GO Annotations	Cellular Component	Nucleus Nucleoplasm Nucleolus Cytoplasm Membrane NLS-dependent Protein Nuclear Import Complex Intracellular Membrane-bounded Organelle	Nucleus Nucleoplasm Transcription Regulator Complex
	Molecular Function	Transcription Corepressor Activity RNA Binding Transcription Factor Binding Sequence-specific DNA Binding E-box Binding	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
	Biological Process	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	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
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		14 interacting genes: APP AR DHX30 DUX4 ESR1 HOXB9 JUN MYB NR2E3 PCNA PPARGC1A PTEN TP53 UBE2I	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
Entrez ID		10514	10002
HPRD ID		05349	05132
Ensembl ID		ENSG00000132382	ENSG00000278570
Uniprot IDs		Q9BQG0	F1D8Q9 Q9Y5X4
PDB IDs			4LOG
Enriched GO Terms of Interacting Partners?
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