FAM86C1P and SMYD1

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

Data Source:
BioGRID (two hybrid)

		FAM86C1P	SMYD1
Description		family with sequence similarity 86 member C1, pseudogene	SET and MYND domain containing 1
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Protein-containing Complex	Nucleus Cytoplasm
	Molecular Function	Protein Binding Protein-L-histidine N-tele-methyltransferase Activity	DNA Binding Transcription Corepressor Activity Protein Binding Histone-lysine N-methyltransferase Activity Metal Ion Binding
	Biological Process	Peptidyl-histidine Methylation, To Form Tele-methylhistidine	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
Pathways
Drugs
Diseases
GWAS			Night sleep phenotypes ( 27126917) Retinal detachment or retinal break ( 31816047)
Interacting Genes		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	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
Entrez ID		55199	150572
HPRD ID		13337	06025
Ensembl ID			ENSG00000115593
Uniprot IDs		Q9NVL1	E9PHG3 Q5HYE8 Q8NB12
PDB IDs
Enriched GO Terms of Interacting Partners?
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