ID   Me32A-DmATP7
AC   CVCL_A8QS
DR   Wikidata; Q108820892
RX   PubMed=20372979;
CC   Sequence variation: Mutation; HGNC; HGNC:869; ATP7A; Unexplicit; 4bp deletion within exon 6; Zygosity=Unspecified (from parent cell line).
CC   Genetic integration: Method=Transfection; Gene=FlyBase_Gene; FBgn0030343; ATP7 (Note=With a N-terminal Myc tag).
CC   Genetic integration: Method=Transfection; Gene=UniProtKB; P00552; Transposon Tn5 neo.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75486; Menkes disease
DI   ORDO; Orphanet_565; Menkes disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_UT42 ! Me32a
CA   Finite cell line
DT   Created: 23-09-21; Last updated: 19-12-24; Version: 5
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RX   PubMed=20372979; DOI=10.1007/s10534-010-9332-2;
RA   Southon A., Palstra N., Veldhuis N., Gaeth A., Robin C., Burke R.,
RA   Camakaris J.;
RT   "Conservation of copper-transporting P(IB)-type ATPase function.";
RL   BioMetals 23:681-694(2010).
//