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FLASH GENE
Symbol FLRT2 contributors: mct - updated : 25-10-2018
HGNC name fibronectin leucine rich transmembrane protein 2
HGNC id 3761
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
2 - 7185 74 660 - 1999 10644439
EXPRESSION
Type
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Cardiovascularheart    
Endocrinepancreas    
Nervousbrain    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Epithelialsecretoryglandularendocrine 
Epithelialsecretoryglandularexocrine 
Muscularstriatumskeletal  
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period embryo
Text widely expressed in the developing embryo, particularly highly expressed initially in the cranial neural crest cells, and later expressed in the developing pharyngeal region
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • ten leucine rich repeats
  • N and C terminal cysteine rich regions
  • one fibronectin-collagen-like domains
  • a transmembrane segment (TM1)
  • an intracellular tail
  • conjugated GlycoP
    HOMOLOGY
    intraspecies paralog to FLRT1
    paralog to FLRT3
    Homologene
    FAMILY
  • fibronectin leucine rich transmembrane protein (FLRT) family
  • CATEGORY adhesion , receptor membrane
    SUBCELLULAR LOCALIZATION extracellular
        plasma membrane
    text type I membrane protein
    basic FUNCTION
  • functioning in cell adhesion and/or receptor signaling
  • FLRT1, FLRT2, FLRT3 have a dual role, promoting FGF signalling and modulating homotypic cell adhesion
  • FLRT proteins act potentially as regulators of FGF signalling, being induced by the signal and then able to interact with the signalling receptor, in many tissues (
  • important roles for FLRT2 and FLRT3 in mediating events such as neural crest cell migration, chondrogenesis and epithelial-mesenchymal interactions during craniofacial development
  • having dual properties as regulators of cell adhesion and potentiators of fibroblast growth factor (FGF) mediated signalling
  • FLRT2 or FLRT3 are potentially required in the epicardium to promote heart morphogenesis
  • plays a role in mediating cell proliferation and cell-cell interactions during early chondrogenesis
  • role of FLRT2 in enhancing cell proliferation and reducing intercellular adhesion during the early stages of chondrogenesis
  • FLRT2, FLRT3 are required for the proper distribution of interneurons within the cortical migratory streams and for the final laminar allocation in the postnatal cortex
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
  • constituent of extracellular matrix
  • INTERACTION
    DNA
    RNA
    small molecule
    protein
  • interacting with UNC5D (FLRT2/UNC5D signalling modulates cortical neuron migration)
  • UNC5D interacts with FLRT2 in cis, controlling cell adhesion in response to externally presented
  • ADGRL2 ligands, such as FLRT2, may be therapeutically exploited to interfere with cancer metastatic dissemination
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS
  • mouse embryos lacking Flrt2 expression arrest at mid-gestation owing to cardiac insufficiency