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FLASH GENE
Symbol ATP10A contributors: mct - updated : 29-06-2021
HGNC name ATPase, Class V, type 10A
HGNC id 13542
EXPRESSION
Type restricted
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Reproductivemale systemtestis  specific Homo sapiens
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period fetal
Text brain, skin
IMPRINTING paternally
text imprinted in brain (monoallelic expressionis variable, and influenced by both gender and common genetic variation)
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
three highly conserved motifs diagnostic of the type 4 subfamily of P-type ATPases
HOMOLOGY
interspecies ortholog to murine Atp10a
ortholog to rattus Atp10a predicted
Homologene
FAMILY
  • cation transport ATPase family
  • class V of the third subfamily of P-type ATPases
  • CATEGORY enzyme , transport carrier
    SUBCELLULAR LOCALIZATION     plasma membrane
        intracellular
    intracellular,cytoplasm,organelle,membrane
    intracellular,cytoplasm,organelle,endoplasmic reticulum
    text
  • integral to membrane
  • basic FUNCTION
  • aminophospholipid and calcium transporting gene
  • may contribute to the Angelman syndrome phenotype
  • translocates phosphatidylcholine and is involved in plasma membrane dynamics
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS active transport
    text
  • cation transport
  • PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule metal binding, nucleotide,
  • ATP
  • Mg2+
  • protein
  • ATP8B1, ATP8B2, and ATP10A transport phosphatidylcholine but not aminophospholipids
  • ATP10A is delivered to the plasma membrane via its interaction with TMEM30A and, specifically, flips phosphatidylcholine (PC) at the plasma membrane
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) AS
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    constitutional   deletion    
    included in PWS/AS typically deleted region, maternally expressed gene
    constitutional     --other  
    dysregulation contributes to some of the obesity-related complications in PWS and in individuals with 15q11-q13 duplication
    constitutional     --over  
    in Hereditary spastic paraplegias (HSPs) with intellectual disability (ID)
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS
  • deficiency of Atp10a and Atp10d leads to insulin resistance and obesity in mice