SPRED1 and BLZF1

Data Source:
BioGRID (two hybrid)

		SPRED1	BLZF1
Description		sprouty related EVH1 domain containing 1	basic leucine zipper nuclear factor 1
Image			No pdb structure
GO Annotations	Cellular Component	Nucleoplasm Cytosol Plasma Membrane Caveola Cytoplasmic Vesicle	Golgi Membrane Nucleus Nucleoplasm Cytoplasm Golgi Apparatus
	Molecular Function	Stem Cell Factor Receptor Binding Protein Binding Protein Kinase Binding Phosphatase Binding Protein Serine/threonine Kinase Inhibitor Activity	Protein Binding Enzyme Binding Ubiquitin Protein Ligase Binding
	Biological Process	MAPK Cascade Inactivation Of MAPK Activity Negative Regulation Of Protein Kinase Activity Fibroblast Growth Factor Receptor Signaling Pathway Negative Regulation Of Epithelial To Mesenchymal Transition Negative Regulation Of Peptidyl-threonine Phosphorylation Negative Regulation Of Phosphatase Activity Negative Regulation Of Angiogenesis Negative Regulation Of Transforming Growth Factor Beta Receptor Signaling Pathway Regulation Of MAPK Cascade Negative Regulation Of MAPK Cascade Positive Regulation Of DNA Damage Response, Signal Transduction By P53 Class Mediator Vasculogenesis Involved In Coronary Vascular Morphogenesis Negative Regulation Of ERK1 And ERK2 Cascade Negative Regulation Of Cell Migration Involved In Sprouting Angiogenesis Regulation Of Protein Deacetylation Negative Regulation Of Lens Fiber Cell Differentiation	Golgi Organization Golgi To Plasma Membrane Protein Transport
Pathways		Regulation of RAS by GAPs FGFRL1 modulation of FGFR1 signaling RAS signaling downstream of NF1 loss-of-function variants	Golgi Cisternae Pericentriolar Stack Reorganization
Drugs
Diseases		Noonan syndrome and related disorders, including: Noonan syndrome (NS); Leopard syndrome (LS); Noonan syndrome-like with loose anagen hair (NS/LAH); CBL-mutation associated syndrome (CBL); Neurofibromatosis type 1 (NF1); Neurofibromatosis type 2 (NF2); Neurofibromatosis-Noonan syndrome (NFNS); Legius syndrome; Cardiofaciocutaneous syndrome (CFCS); Costello syndrome (CS)
GWAS		Bipolar disorder ( 20351715) Birth weight ( 31043758) Cognitive performance (processing speed) ( 31598132) Crohn's disease ( 23128233) Erosive tooth wear (severe vs non-severe) ( 29898447) Erosive tooth wear (severe vs none or mild) ( 29898447) HDL cholesterol levels x long total sleep time interaction (2df test) ( 31719535) Hypersomnia (HLA-DQB1*06:02 negative) ( 23646285)
Interacting Genes		37 interacting genes: ANKS1A AQP1 BEX2 BLZF1 C2orf68 CCDC185 CDKN1A CREB5 DNAJB11 FAM118B FAM90A1 GLYCTK HEXIM2 HPCAL4 HSF2BP IL16 KIT MAB21L3 MEOX2 NAGK NCALD OSGEP PIH1D2 PPP1CA PPP1R7 PRPF18 RCC1 RIN1 SPG21 SUV39H1 TSC22D1 TTC19 VSNL1 ZNF408 ZNF417 ZNF587 ZNF655	101 interacting genes: AKAP9 AMOTL2 ANKS1A AQP1 BAG4 BANP BCL6 BEX2 CARD9 CCDC120 CCDC33 CCNH CDC37 CDK18 CFAP206 CHCHD3 CINP CKS2 CTNNA3 DNMT3L ENKD1 ERCC3 EWSR1 EXOC8 FAM124B FAM90A1 FBF1 FHL2 FRMD6 FRS3 GEM GORASP2 HCLS1 HDAC4 HOXA1 HOXC8 IGFN1 IKZF3 IL16 IQUB KANK2 KAT5 KCTD9 KDM1A KIF9 KLHL38 LGALS14 LMO1 LMO2 LMO3 LNX1 MID2 MISP MKRN3 NTAQ1 OAZ3 PCDHB12 PIK3R3 PKN1 POLR1C PRKAB2 PRMT6 PRPF18 PSMA1 PTPN11 RAB2A RAB2B RAB39A RANBP3 RHOJ SCNM1 SMAD3 SMARCB1 SPRED1 SRA1 SSX2 SUV39H2 SYT17 TBC1D22B TBC1D7 TCAP TCF19 TEKT4 TNS2 TRAPPC2L TRIM59 TSC22D4 TSTD2 TTC23 TXNDC5 USHBP1 VPS28 ZBTB16 ZBTB24 ZGPAT ZMAT1 ZNF124 ZNF410 ZNF688 ZNF76 ZZZ3
Entrez ID		161742	8548
HPRD ID		11601	16367
Ensembl ID		ENSG00000166068	ENSG00000117475
Uniprot IDs		Q7Z699	Q9H2G9
PDB IDs		3SYX 6V65 6V6F
Enriched GO Terms of Interacting Partners?
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