ID   MDS-2.13
AC   CVCL_VH19
DR   GEO; GSM1594193
DR   Wikidata; Q54904820
RX   PubMed=25798938;
CC   Omics: Deep exome analysis.
CC   Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
CC   Cell type: Mononuclear cell; CL=CL_0000842.
ST   Source(s): PubMed=25798938
ST   Amelogenin: X,Y
ST   CSF1PO: 11
ST   D13S317: 11
ST   D16S539: 11,13
ST   D19S433: 13,15
ST   D21S11: 29,32.2
ST   D2S1338: 16,23
ST   D3S1358: 14,15
ST   D5S818: 12,13
ST   D7S820: 10,12
ST   D8S1179: 12,15
ST   FGA: 23
ST   TH01: 6,9.3
ST   TPOX: 8,10
ST   vWA: 17
DI   NCIt; C3247; Myelodysplastic syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_VH20 ! MDS-2.A3
OI   CVCL_VH22 ! N-2.8
OI   CVCL_VH21 ! N-2.12
OI   CVCL_VH24 ! N-2.A2
OI   CVCL_VH23 ! N-2.A11
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 29-06-23; Version: 6
//
RX   PubMed=25798938; DOI=10.1038/nbt.3178; PMCID=PMC4464949;
RA   Kotini A.G., Chang C.-J., Boussaad I., Delrow J.J., Dolezal E.K.,
RA   Nagulapally A.B., Perna F., Fishbein G.A., Klimek V.M., Hawkins R.D.,
RA   Huangfu D.-W., Murry C.E., Graubert T.A., Nimer S.D., Papapetrou E.P.;
RT   "Functional analysis of a chromosomal deletion associated with
RT   myelodysplastic syndromes using isogenic human induced pluripotent
RT   stem cells.";
RL   Nat. Biotechnol. 33:646-655(2015).
//