RINT1 and DCX

Number of citations of the paper that reports this interaction (PMID 25416956)
0

Data Source:
BioGRID (two hybrid)

		RINT1	DCX
Gene Name		RAD50 interactor 1	doublecortin
Image		No pdb structure
Gene Ontology Annotations	Cellular Component	Endoplasmic Reticulum Endoplasmic Reticulum Membrane	Cytosol Cytoskeleton Microtubule Microtubule Associated Complex Neuron Projection
	Molecular Function	Protein Binding	Protein Binding Microtubule Binding Protein Kinase Binding
	Biological Process	Cell Cycle Protein Transport Golgi Vesicle Transport Regulation Of ER To Golgi Vesicle-mediated Transport Regulation Of Signal Transduction Involved In Mitotic G2 DNA Damage Checkpoint	Neuron Migration Nervous System Development Axon Guidance Central Nervous System Development Brain Development Central Nervous System Projection Neuron Axonogenesis Intracellular Signal Transduction Axon Extension Dendrite Morphogenesis
Pathways			Axon guidance Neurofascin interactions L1CAM interactions
Drugs
Diseases
GWAS
Protein-Protein Interactions		43 interactors: ARNT2 BNIP3L C1orf109 CCDC101 CCDC121 CCDC146 CEP57L1 CSPP1 CWF19L2 DCX EPC1 FAM107A FAM110A FAM124B FAM161A FAM81B FAM90A1 GFI1B HDAC4 LMO2 LSP1P3 PIK3R2 RAD50 RB1 RBL1 RBL2 RBM41 RIBC1 RSRC2 RTP5 SCNM1 SFR1 SH2D4A SMARCE1 SNW1 SPTBN1 STRN TXLNA VPS37C XPNPEP1 ZNF655 ZNF697 ZW10	29 interactors: ACD AP1M1 AP2M1 APP CALCOCO2 CDK5 FBXO25 GOLGA2 IKZF1 KIFC3 KRT40 KRTAP10-8 MEOX1 MID2 NFASC PAFAH1B1 POT1 PPP1CA PPP1R9B RINT1 SPAG5 SPP1 TERF1 TINF2 TRIM23 TRIM27 TRIM39 USP9X ZBTB5
Entrez ID		60561	1641
HPRD ID		15250	02127
Ensembl ID		ENSG00000135249	ENSG00000077279
Uniprot IDs		Q6NUQ1	A8K340 B4DM53 O43602
PDB IDs			1MJD 2BQQ 2XRP 4ATU
Enriched GO Terms of Interacting Partners?		Chromosome Organization Chromatin Modification Regulation Of Lipid Kinase Activity Chromatin Organization Protein Localization To Chromosome Regulation Of Transcription From RNA Polymerase II Promoter Transcription, DNA-templated RNA Biosynthetic Process Positive Regulation Of Transcription From RNA Polymerase II Promoter Gene Expression Organelle Organization RNA Metabolic Process Protein Localization To Chromosome, Centromeric Region Cellular Nitrogen Compound Metabolic Process Nucleobase-containing Compound Metabolic Process Positive Regulation Of Transcription, DNA-templated Cellular Macromolecule Biosynthetic Process Macromolecule Biosynthetic Process Heterocycle Metabolic Process Cellular Aromatic Compound Metabolic Process Negative Regulation Of Transcription, DNA-templated Regulation Of Transcription, DNA-templated Negative Regulation Of Transcription From RNA Polymerase II Promoter Regulation Of Nucleic Acid-templated Transcription Regulation Of Histone H3-K4 Methylation Negative Regulation Of Nucleic Acid-templated Transcription Nitrogen Compound Metabolic Process Regulation Of RNA Biosynthetic Process Positive Regulation Of Macromolecule Biosynthetic Process Regulation Of Nitrogen Compound Metabolic Process Negative Regulation Of RNA Biosynthetic Process Regulation Of Lipid Metabolic Process Positive Regulation Of Gene Expression Regulation Of RNA Metabolic Process Mitotic Metaphase Plate Congression Viral Process Positive Regulation Of Cellular Biosynthetic Process Metaphase Plate Congression Regulation Of Cell Cycle Negative Regulation Of Gene Expression Negative Regulation Of Biosynthetic Process Biosynthetic Process Regulation Of Gene Expression Establishment Of Chromosome Localization Microtubule Anchoring Chromatin Remodeling Regulation Of Histone Methylation Regulation Of Chromosome Organization Mitotic Cell Cycle Positive Regulation Of Vitamin D Receptor Signaling Pathway	Negative Regulation Of Telomere Maintenance Via Telomerase Negative Regulation Of Telomere Maintenance Regulation Of Telomere Maintenance Via Telomerase Regulation Of Telomere Maintenance Telomere Assembly Negative Regulation Of DNA Replication Regulation Of Telomerase Activity Negative Regulation Of Cellular Metabolic Process Telomere Maintenance Cell Cycle Negative Regulation Of Chromosome Organization Regulation Of Cellular Component Organization Negative Regulation Of DNA Metabolic Process Regulation Of Organelle Organization Cell Division Telomere Maintenance Via Telomere Lengthening Negative Regulation Of Biosynthetic Process Organelle Organization Regulation Of DNA Replication Regulation Of Developmental Growth Protein Localization To Chromosome, Telomeric Region Telomere Capping Regulation Of DNA Biosynthetic Process Movement Of Cell Or Subcellular Component Axonogenesis Cellular Component Assembly Protein Localization Positive Regulation Of Telomerase Activity Neuron Projection Development Cellular Localization Axon Development Cell Morphogenesis Involved In Neuron Differentiation Locomotion Regulation Of Growth Telomere Maintenance Via Telomerase Negative Regulation Of Telomerase Activity Negative Regulation Of Neuron Differentiation Neuron Projection Morphogenesis Neuron Development Immune System Process Positive Regulation Of Telomere Maintenance Hippocampus Development Positive Regulation Of Organelle Organization Regulation Of Chromosome Organization Regulation Of Mitotic Cell Cycle Cell Morphogenesis Involved In Differentiation Forebrain Development Developmental Cell Growth Negative Regulation Of Viral Release From Host Cell Neuron Differentiation
Tagcloud ?		apparatus autophagy checkpoint comprises counterpart cytokinesis decay discuss dsl1 dsl3 endoplasmic endosome golgi intercorrelation metazoan moonlighting nag nrz participate reticulum retrograde sec39 summarize tethering tip20 trafficking transport vesicle zw10	17p13 classical deletions disrupt epilepsy frontal gradient lis lis1 lissencephaly malformation mutations occipital overlapping parietal proline q23 repeats retardation sequencing sexes southern splice sporadic though truncation wd40 xlis xq22
Tagcloud (Difference) ?		apparatus autophagy checkpoint comprises counterpart cytokinesis decay discuss dsl1 dsl3 endoplasmic endosome golgi intercorrelation metazoan moonlighting nag nrz participate reticulum retrograde sec39 summarize tethering tip20 trafficking transport vesicle zw10	17p13 classical deletions disrupt epilepsy frontal gradient lis lis1 lissencephaly malformation mutations occipital overlapping parietal proline q23 repeats retardation sequencing sexes southern splice sporadic though truncation wd40 xlis xq22
Tagcloud (Intersection) ?