SIX5

Description		SIX homeobox 5
Image		No pdb structure
GO Annotations	Cellular Component	Nuclear Chromatin Nucleus Transcription Factor Complex Cytoplasm
	Molecular Function	Transcription Regulatory Region Sequence-specific DNA Binding RNA Polymerase II Proximal Promoter Sequence-specific DNA Binding DNA-binding Transcription Factor Activity, RNA Polymerase II-specific DNA-binding Transcription Activator Activity, RNA Polymerase II-specific Protein Binding
	Biological Process	Lens Development In Camera-type Eye Spermatid Development Negative Regulation Of Transcription, DNA-templated Positive Regulation Of Transcription By RNA Polymerase II Anatomical Structure Development Negative Regulation Of Skeletal Muscle Satellite Cell Proliferation
Pathways
Drugs
Diseases		Contiguous gene deletion syndrome involving EYA1, including: Oto-facio-cervical syndrome (OFC); Branchiootic syndrome 1 (BOS1); Branchio-oto-renal syndrome (BOR)
GWAS		Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) ( 30940143)
Interacting Genes		3 interacting genes: ATXN1 EYA3 HMGB1
Entrez ID		147912
HPRD ID		09024
Ensembl ID		ENSG00000177045
Uniprot IDs		Q8N196
PDB IDs
Enriched GO Terms of Interacting Partners?
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