ID   iMPD562.C2
AC   CVCL_D187
SY   iPS MPD562 clone 2; iPS MPD 562 clone 2
DR   SKIP; SKIP000530
DR   Wikidata; Q54897615
RX   PubMed=19797525;
CC   From: Johns Hopkins University School of Medicine; Baltimore; USA.
CC   Sequence variation: Mutation; HGNC; HGNC:6192; JAK2; Simple; p.Val617Phe (c.1849G>T); ClinVar=VCV000014662; Zygosity=Heterozygous (PubMed=19797525).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C4345; Myeloproliferative neoplasm
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_D188 ! iMPD562.C3
SX   Female
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 22-10-12; Last updated: 19-12-24; Version: 16
//
RX   PubMed=19797525; DOI=10.1182/blood-2009-04-217406; PMCID=PMC2798863;
RA   Ye Z.-H., Zhan H.-C., Mali P., Dowey S., Williams D.M., Jang Y.-Y.,
RA   Dang C.V., Spivak J.L., Moliterno A.R., Cheng L.-Z.;
RT   "Human-induced pluripotent stem cells from blood cells of healthy
RT   donors and patients with acquired blood disorders.";
RL   Blood 114:5473-5480(2009).
//