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
FHL3 four and a half LIM domains 3
FLNA filamin A
  • Platelet degranulation
  • GP1b-IX-V activation signalling
  • Cell-extracellular matrix interactions
  • RHO GTPases activate PAKs
  • OAS antiviral response
  • Artenimol
  • FG syndrome (FGS); Opitz-Kaveggia syndrome
  • Periventricular nodular heterotopia (PVNH)
  • Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
  • Fronto-Otopalatodigital Osteodysplasia, including: Otopalatodigital syndrome, type I; Otopalatodigital syndrome, type II; Melnick-Needles syndrome; Frontometaphyseal dysplasia
FRMD8 FERM domain containing 8
GAGE12G G antigen 12G
GAGE2E G antigen 2E
GEM GTP binding protein overexpressed in skeletal muscle
  • NPAS4 regulates expression of target genes
GFER growth factor, augmenter of liver regeneration
  • Mitochondrial protein import
  • Flavin adenine dinucleotide
GLUL glutamate-ammonia ligase
  • Astrocytic Glutamate-Glutamine Uptake And Metabolism
  • Glutamate and glutamine metabolism
  • L-Glutamine
  • Glutamic acid
  • Congenital systemic glutamine deficiency (CSGD); Glutamine synthetase deficiency
GNMT glycine N-methyltransferase
  • Metabolism of ingested SeMet, Sec, MeSec into H2Se
  • Glyoxylate metabolism and glycine degradation
  • Developmental Lineage of Pancreatic Acinar Cells
  • Ademetionine
  • Glycine
  • S-adenosyl-L-homocysteine
  • Hypermethioninemia; Methionine adenosyltransferase deficiency; S-adenosylhomocysteine hydrolase deficiency
GPBP1 GC-rich promoter binding protein 1
GPBP1L1 GC-rich promoter binding protein 1 like 1
GRAMD4 GRAM domain containing 4
GTPBP2 GTP binding protein 2
  • Platelet degranulation
HEBP2 heme binding protein 2
  • Neutrophil degranulation
HSPB7 heat shock protein family B (small) member 7
INO80 INO80 complex ATPase subunit
  • UCH proteinases
  • DNA Damage Recognition in GG-NER
KCNAB3 potassium voltage-gated channel subfamily A regulatory beta subunit 3
  • Voltage gated Potassium channels
KCNJ5-AS1 KCNJ5 antisense RNA 1
KRTAP10-10 keratin associated protein 10-10
  • Keratinization
KRTAP5-4 keratin associated protein 5-4
  • Keratinization

Page 4 out of 9 pages