SMYD1 and FAM86C1P

Number of citations of the paper that reports this interaction (PubMedID 32296183)
86

Data Source:
BioGRID (two hybrid)

		SMYD1	FAM86C1P
Description		SET and MYND domain containing 1	family with sequence similarity 86 member C1, pseudogene
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Nucleus Cytoplasm	Protein-containing Complex
	Molecular Function	DNA Binding Transcription Corepressor Activity Protein Binding Histone-lysine N-methyltransferase Activity Metal Ion Binding	Protein Binding Protein-L-histidine N-tele-methyltransferase Activity
	Biological Process	Chromatin Remodeling Heart Development Positive Regulation Of Myotube Differentiation Histone Lysine Methylation Skeletal Muscle Cell Differentiation Positive Regulation Of Myoblast Differentiation Negative Regulation Of Transcription, DNA-templated	Peptidyl-histidine Methylation, To Form Tele-methylhistidine
Pathways
Drugs
Diseases
GWAS		Night sleep phenotypes ( 27126917) Retinal detachment or retinal break ( 31816047)
Interacting Genes		44 interacting genes: ARID5A BACH2 BHLHE40 C11orf1 C11orf16 C11orf53 CCDC113 CCDC33 DISC1 DVL1 FAM166A FAM204A FAM83A FAM86C1P H3-5 HDAC2 HDAC3 HDHD3 HMG20A HOMEZ KIF16B KRT35 LENG8 MDFI MEOX2 MYH7B NACA NEFL OGDHL PATZ1 POU6F2 PRR22 RBM4B RSPH6A RUSC1 SNX11 SPAG8 TBRG1 TTC33 USP54 UTP14A WDR77 ZBTB3 ZBTB44	22 interacting genes: ANKS1A BCAS2 C1orf109 CDKN2D CDR2L COL8A1 CRACR2A CSNK2B CTTNBP2 DOK6 GPSM3 HNRNPF KRT26 KYNU MAGED4B PCSK5 POU4F2 SAT1 SMYD1 SPG21 TRAF1 VENTX
Entrez ID		150572	55199
HPRD ID		06025	13337
Ensembl ID		ENSG00000115593
Uniprot IDs		E9PHG3 Q5HYE8 Q8NB12	Q9NVL1
PDB IDs
Enriched GO Terms of Interacting Partners?
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