CFL1 and CLCN5

Number of citations of the paper that reports this interaction (PubMedID 12904289)
17

Data Source:
HPRD (in vitro, in vivo, two hybrid)

		CFL1	CLCN5
Description		cofilin 1	chloride voltage-gated channel 5
Image
GO Annotations	Cellular Component	Extracellular Space Nucleus Cytoplasm Cytosol Cell-cell Junction Focal Adhesion Membrane Nuclear Matrix Lamellipodium Cortical Actin Cytoskeleton Lamellipodium Membrane Vesicle Ruffle Membrane Extracellular Exosome	Golgi Membrane Lysosomal Membrane Endosome Early Endosome Golgi Apparatus Cytosol Plasma Membrane Integral Component Of Plasma Membrane Synaptic Vesicle Endosome Membrane Membrane Apical Part Of Cell
	Molecular Function	Signaling Receptor Binding Protein Binding Actin Filament Binding	Voltage-gated Chloride Channel Activity Chloride Channel Activity Protein Binding ATP Binding Solute:proton Antiporter Activity Chloride Ion Binding Identical Protein Binding
	Biological Process	Mitotic Cytokinesis Neural Crest Cell Migration Neural Fold Formation Protein Phosphorylation Cytoskeleton Organization Rho Protein Signal Transduction Response To Virus Regulation Of Cell Morphogenesis Establishment Of Cell Polarity Actin Cytoskeleton Organization Actin Filament Depolymerization Actin Filament Fragmentation Positive Regulation Of Actin Filament Depolymerization Interleukin-12-mediated Signaling Pathway Negative Regulation Of Apoptotic Process Response To Amino Acid Positive Regulation By Host Of Viral Process Regulation Of Dendritic Spine Morphogenesis	Excretion Ion Transmembrane Transport Chloride Transmembrane Transport Proton Transmembrane Transport
Pathways		Platelet degranulation Regulation of actin dynamics for phagocytic cup formation EPHB-mediated forward signaling Sema3A PAK dependent Axon repulsion RHO GTPases Activate ROCKs Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation	Stimuli-sensing channels
Drugs		Lauryl Dimethylamine-N-Oxide Copper Artenimol
Diseases			Dent disease, including: Dent disease 1; Dent disease 2; X-linked recessive nephrolithiasis ; Hypophosphatemic rickets; Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis
GWAS		Acne (severe) ( 24927181) Basal cell carcinoma ( 31174203) Breast cancer ( 23535729) DNA methylation (variation) ( 23725790) Keratinocyte cancer (MTAG) ( 31174203) Psoriasis ( 28537254)	Height ( 28552196) Hip circumference adjusted for BMI ( 28552196)
Interacting Genes		40 interacting genes: ACTA1 ACTA2 ACTB ACTC1 ACTG1 APP ATP1A1 ATXN1 CFL2 CLCN5 EGFR ESR1 HSPH1 LIMK1 LIMK2 MAPK6 MAPK8IP2 MYCBP NRK POT1 PSEN1 PTEN RAD21 RPS6KA1 SLC2A4 SRC SSH1 SSH2 SSH3 TAB1 TERF1 TESK1 TESK2 TPI1 TRIM15 UCHL5 WDR1 YWHAG YWHAQ YWHAZ	4 interacting genes: CFL1 MAGI1 WWP1 WWP2
Entrez ID		1072	1184
HPRD ID		03261	02053
Ensembl ID		ENSG00000172757	ENSG00000171365
Uniprot IDs		P23528 V9HWI5	A8K4H5 B3KRR2 P51795 V9GYG7
PDB IDs		1Q8G 1Q8X 3J0S 4BEX 5HVK 5L6W	2J9L 2JA3
Enriched GO Terms of Interacting Partners?
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