PHF6

Description		PHD finger protein 6
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GO Annotations	Cellular Component	Condensed Chromosome Kinetochore Nucleus Nucleoplasm Nucleolus
	Molecular Function	DNA Binding RNA Binding Protein Binding Tubulin Binding Enzyme Binding Histone Binding Histone Deacetylase Binding Ribonucleoprotein Complex Binding Metal Ion Binding Phosphoprotein Binding Scaffold Protein Binding
	Biological Process	Negative Regulation Of Transcription By RNA Polymerase II Regulation Of Transcription By RNA Polymerase II
Pathways
Drugs
Diseases		Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
GWAS
Interacting Genes		1 interacting genes: SRPK2
Entrez ID		84295
HPRD ID		02330
Ensembl ID		ENSG00000156531
Uniprot IDs		Q8IWS0
PDB IDs		4NN2 4R7A
Enriched GO Terms of Interacting Partners?
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