CDR2L and FAM86C1P

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

		CDR2L	FAM86C1P
Description		cerebellar degeneration related protein 2 like	family with sequence similarity 86 member C1, pseudogene
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component		Protein-containing Complex
	Molecular Function	Protein Binding Identical Protein Binding	Protein Binding Protein-L-histidine N-tele-methyltransferase Activity
	Biological Process		Peptidyl-histidine Methylation, To Form Tele-methylhistidine
Pathways
Drugs
Diseases
GWAS		Alzheimer's disease in APOE e4- carriers ( 25778476) Bipolar disorder ( 31043756)
Interacting Genes		61 interacting genes: ANKRD11 BFSP2 C1orf216 C4orf46 C9orf24 CCDC146 CCDC153 CCDC185 CCDC187 CCHCR1 CDR2 COX5B EHHADH ELOA FAIM FAM161A FAM161B FAM86C1P HDAC4 HSF2BP INO80B KRT31 KRTAP13-4 LENG1 MESD OIP5 PPP1R18 PRPF31 PSME3 RASAL3 RASD1 REL RINT1 SCNM1 SH2D4A SPRY1 STX11 TBRG4 TCEANC TCHP TCP10L TFIP11 TSGA10IP UBE2I WASHC1 ZBTB42 ZNF19 ZNF250 ZNF35 ZNF417 ZNF572 ZNF629 ZNF648 ZNF655 ZNF669 ZNF688 ZNF80 ZNF835 ZSCAN22 ZSCAN23 ZSCAN26	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		30850	55199
HPRD ID		11041	13337
Ensembl ID		ENSG00000109089
Uniprot IDs		A0A024R8R6 Q86X02	Q9NVL1
PDB IDs
Enriched GO Terms of Interacting Partners?
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