CRTAP and MIR199A2

Data Source:
BioGRID (unspecified method)

		CRTAP	MIR199A2
Description		cartilage associated protein	microRNA 199a-2
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Extracellular Space Endoplasmic Reticulum Endoplasmic Reticulum Lumen Protein-containing Complex
	Molecular Function	Protein Binding Collagen Binding
	Biological Process	Spermatogenesis Peptidyl-proline Hydroxylation To 3-hydroxy-L-proline Collagen Fibril Organization Protein Stabilization Chaperone-mediated Protein Folding Negative Regulation Of Post-translational Protein Modification	Gene Silencing By MiRNA
Pathways		Collagen biosynthesis and modifying enzymes
Drugs
Diseases		Osteogenesis imperfecta
GWAS		Asthma ( 31959851 31619474) Major depressive disorder ( 29317602) Multiple sclerosis ( 31604244) Refractive error ( 32231278) Retinal detachment or retinal break ( 31816047)
Interacting Genes		24 interacting genes: MIR1-1 MIR10B MIR128-1 MIR138-2 MIR140 MIR16-1 MIR16-2 MIR17 MIR18A MIR199A2 MIR19A MIR19B1 MIR200B MIR200C MIR20A MIR9-1 MIR9-2 MIR9-3 MIR92A1 MIRLET7B MIRLET7E MIRLET7F2 MIRLET7G MIRLET7I	75 interacting genes: ADARB1 AIMP1 APOBEC3B AQR C1QBP CPSF1 CRTAP DARS1 DDX1 DDX21 DDX3X DHX36 EIF2AK2 EPRS1 ERAL1 FAM98A FAM98B FUS HNRNPA0 HNRNPA1 HNRNPA2B1 HNRNPA3 HNRNPF HNRNPH1 HNRNPH2 HNRNPH3 HNRNPK HNRNPL HNRNPM HNRNPR IARS1 IGF2BP1 IGF2BP2 IGF2BP3 KNOP1 LARP7 LIN28A LRPPRC MARS1 MATR3 MSI2 NOL6 NONO NUDT21 PDCD11 PLOD1 PRMT1 PTBP1 PTBP3 PUF60 PUM1 PUM2 QARS1 RARS1 RBFOX2 RBM14 RTCA RTCB SF3A1 SF3B1 SF3B2 SF3B3 SFPQ SPOUT1 STRBP SYNCRIP TAF15 TRA2A TRA2B U2SURP UPF1 UTP20 YBX1 YBX2 YBX3
Entrez ID		10491	406977
HPRD ID		16110
Ensembl ID		ENSG00000170275	ENSG00000208024
Uniprot IDs		O75718
PDB IDs
Enriched GO Terms of Interacting Partners?
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