STX11 and SLC38A2

Number of citations of the paper that reports this interaction (PubMedID 16169070)
820

Data Source:
BioGRID (two hybrid)
HPRD (two hybrid)

		STX11	SLC38A2
Description		syntaxin 11	solute carrier family 38 member 2
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Golgi Apparatus Plasma Membrane Synaptic Vesicle Endomembrane System Integral Component Of Membrane SNARE Complex Presynaptic Membrane Presynaptic Active Zone Membrane	Plasma Membrane Integral Component Of Plasma Membrane Brush Border Axon Dendrite Sarcolemma Neuronal Cell Body
	Molecular Function	SNARE Binding SNAP Receptor Activity Protein Binding	Protein Binding Amino Acid Transmembrane Transporter Activity L-glutamine Transmembrane Transporter Activity L-serine Transmembrane Transporter Activity Symporter Activity
	Biological Process	Intracellular Protein Transport Exocytosis Vesicle Fusion Synaptic Vesicle Fusion To Presynaptic Active Zone Membrane Vesicle Docking Membrane Fusion	Amino Acid Transmembrane Transport Sodium Ion Transport Amino Acid Transport Glutamine Transport Female Pregnancy Positive Regulation Of Gene Expression Glutamate Secretion L-serine Transport Cerebral Cortex Development Glycine Betaine Transport Alanine Transport Positive Regulation Of RNA Splicing Cellular Response To Amino Acid Starvation Cellular Response To Mechanical Stimulus Regulation Of Cellular Response To Stress Cellular Response To Arsenite(3-)
Pathways			Glutamate Neurotransmitter Release Cycle Amino acid transport across the plasma membrane
Drugs
Diseases		Familial hemophagocytic lymphohistiocytosis (FHPL), including the following three diseases: Perforin deficiency; Munc deficiency; STX11 deficiency
GWAS		Pre-treatment viral load in HIV-1 infection ( 31219150)	Blond vs. brown/black hair color ( 30531825) Uterine fibroids ( 31649266)
Interacting Genes		64 interacting genes: APP AXIN1 BLOC1S6 BYSL C1orf109 CARD9 CCBE1 CCDC184 CCDC33 CCNK CDCA7L CRYBA4 CTBP2 CWF19L2 EIF1AD FAM110A FAM161A FAM74A4 FAM90A1 FARS2 GOLGA8EP GOLGA8F HAUS1 HGS IKBKG IKZF3 KAT5 KCTD9 KDM1A KLC3 KXD1 LENG1 LONRF1 MBIP MEOX2 MFAP1 MID2 NDC80 NTAQ1 PPP1R18 PRKAB2 PRPF31 PSMA3 PSMC3 RNF6 RUNX1T1 SH2D4A SLC38A2 SMARCE1 SNAP23 SNAP25 SNX3 SUV39H1 TAF6L TBK1 TCF4 TLE5 TNFRSF21 USHBP1 VAMP2 VPS52 ZCCHC10 ZNF417 ZNF587	2 interacting genes: APP STX11
Entrez ID		8676	54407
HPRD ID		09231	05535
Ensembl ID		ENSG00000135604	ENSG00000134294
Uniprot IDs		O75558	A0A024R0W3 Q8NHT5 Q96QD8
PDB IDs
Enriched GO Terms of Interacting Partners?
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