FAM86C1P and CDR2L

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

		FAM86C1P	CDR2L
Description		family with sequence similarity 86 member C1, pseudogene	cerebellar degeneration related protein 2 like
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Protein-containing Complex
	Molecular Function	Protein Binding Protein-L-histidine N-tele-methyltransferase Activity	Protein Binding Identical Protein Binding
	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		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	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
Entrez ID		55199	30850
HPRD ID		13337	11041
Ensembl ID			ENSG00000109089
Uniprot IDs		Q9NVL1	A0A024R8R6 Q86X02
PDB IDs
Enriched GO Terms of Interacting Partners?
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