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FLASH GENE
Symbol SLC24A5 contributors: mct/npt - updated : 12-07-2023
HGNC name solute carrier family 24, member 5
HGNC id 20611
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • two large hydrophilic loops
  • two sets of transmembrane spanning segments (TMs)
  • the first large hydrophilic loop is located extracellularly at the N-terminus
  • the other is cytoplasmic and separates the two sets of TMs (Kinjo 2003)
  • HOMOLOGY
    interspecies homolog to murine F630045L20Rik
    Homologene
    FAMILY
  • sodium/potassium/calcium exchanger family
  • SLC24A subfamily
  • SLC24A subfamily
  • CATEGORY transport carrier
    SUBCELLULAR LOCALIZATION     plasma membrane
        intracellular
    intracellular,cytoplasm,organelle,mitochondria
    intracellular,cytoplasm,organelle,Golgi
    text
  • partially localized to the trans-Golgi network of epidermal melanocytes
  • localize either in the trans-Golgi network (TGN) or in melanosomes
  • localized to mitochondria, not to melanosomes
  • basic FUNCTION
  • may be functioning in the removal and maintenance of calcium homeostasis during signaling in the adult and in signaling events during embryogenesis and patterning of imaginal disks
  • may have a key role in skin pigmentation possibly by participating to ion transport in melanosomes
  • probably transports one Ca2+ and one K+ in exchange for four Na+
  • playing a role in mediating agonist-stimulated [Ca2+]cyt and thereby vascular tone (Dong 2006)
  • directly regulating epidermal melanogenesis and natural skin color through its intracellular potassium-dependent exchanger activity
  • polytopic membrane protein that plays a critical role in Ca(2+) homeostasis in retinal rod and cone photoreceptors (Kinjo 2003)
  • probably play a particularly prominent role in regulating Ca2+ flux in environments which experience wide and frequent fluctuations in Na+ concentration (Lytton 2007)
  • is involved in the maturation of melanosomes
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
  • ion Ca2+
  • ion K+
  • ion Na+
  • protein
    cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) OCA6
    Susceptibility to natural skin color variation
    Variant & Polymorphism SNP non-synonymous single nucleotide polymorphism associated with natural skin color variation
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS