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Cellosaurus Me32A-DmATP7 (CVCL_A8QS)

[Text version]
Cell line name Me32A-DmATP7
Accession CVCL_A8QS
Resource Identification Initiative To cite this cell line use: Me32A-DmATP7 (RRID:CVCL_A8QS)
Comments Genetic integration: Method=Transfection; Gene=FlyBase_Gene; FBgn0030343; ATP7 (Note=With a N-terminal Myc tag).
Genetic integration: Method=Transfection; Gene=UniProtKB; P00552; Transposon Tn5 neo.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:869; ATP7A; Unexplicit; 4bp deletion within exon 6; Zygosity=Unspecified (from parent cell line).
Disease Menkes disease (NCIt: C75486)
Menkes disease (ORDO: Orphanet_565)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_UT42 (Me32a)
Category Finite cell line
Publications

PubMed=20372979; DOI=10.1007/s10534-010-9332-2
Southon A., Palstra N., Veldhuis N., Gaeth A., Robin C., Burke R., Camakaris J.
Conservation of copper-transporting P(IB)-type ATPase function.
BioMetals 23:681-694(2010)

Cross-references
Encyclopedic resources Wikidata; Q108820892
Entry history
Entry creation23-Sep-2021
Last entry update19-Dec-2024
Version number5