Search Results for: PLEKHF2

176 interactions involving PLEKHF2 - pleckstrin homology and FYVE domain containing 2 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
BCAS2 BCAS2 pre-mRNA processing factor
  • mRNA Splicing - Major Pathway
BCAS3 BCAS3 microtubule associated cell migration factor
BEND7 BEN domain containing 7
BLOC1S6 biogenesis of lysosomal organelles complex 1 subunit 6
  • Golgi Associated Vesicle Biogenesis
BOD1 biorientation of chromosomes in cell division 1
  • Formation of WDR5-containing histone-modifying complexes
BRD7 bromodomain containing 7
  • Regulation of TP53 Activity through Acetylation
  • Formation of the polybromo-BAF (pBAF) complex
BSCL2 BSCL2 lipid droplet biogenesis associated, seipin
  • Congenital generalized lipodystrophy (CGL)
  • Distal hereditary motor neuropathies (dHMN)
  • Hereditary spastic paraplegia (SPG)
C1orf35 chromosome 1 open reading frame 35
  • Neutrophil degranulation
C3 complement C3
  • Alternative complement activation
  • Activation of C3 and C5
  • Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
  • Peptide ligand-binding receptors
  • Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
  • G alpha (i) signalling events
  • Neutrophil degranulation
  • Post-translational protein phosphorylation
  • Purinergic signaling in leishmaniasis infection
  • Regulation of Complement cascade
  • Human immunoglobulin G
  • Zinc
  • S-Hydroxycysteine
  • Mirococept
  • Copper
  • Zinc acetate
  • Zinc chloride
  • Zinc sulfate, unspecified form
  • Pegcetacoplan
  • Macular degeneration, including: Age-related macular degeneration (ARMD); Patterned dystrophy of retinal pigment epithelium (PDREP); Retinal macular dystrophy 2 (MCDR2); X-linked atrophic macular degeneration (MDXLA)
  • Classic complement pathway component defects, including the following eight diseases: C1q alpha-chain deficiency; C1q beta-chain deficiency; C1q gamma-chain deficiency; C1r deficiency; C1s deficiency; C2 deficiency; C3 deficiency; C4 deficiency
CAVIN2 caveolae associated protein 2
CBX8 chromobox 8
  • Oxidative Stress Induced Senescence
  • SUMOylation of DNA damage response and repair proteins
  • SUMOylation of transcription cofactors
  • SUMOylation of chromatin organization proteins
  • SUMOylation of RNA binding proteins
  • SUMOylation of DNA methylation proteins
  • RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
  • Regulation of PTEN gene transcription
  • Regulation of PTEN gene transcription
CCDC146 coiled-coil domain containing 146
CCDC172 coiled-coil domain containing 172
CCDC25 coiled-coil domain containing 25
CCDC85B coiled-coil domain containing 85B
CDC20B cell division cycle 20B
CEP44 centrosomal protein 44
CERK ceramide kinase
  • Glycosphingolipid biosynthesis
CGGBP1 CGG triplet repeat binding protein 1
CHCHD2 coiled-coil-helix-coiled-coil-helix domain containing 2
  • Mitochondrial protein import
  • Mitochondrial protein degradation

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