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Cellosaurus MDS-2.13 (CVCL_VH19)

[Text version]
Cell line name MDS-2.13
Accession CVCL_VH19
Resource Identification Initiative To cite this cell line use: MDS-2.13 (RRID:CVCL_VH19)
Comments Omics: Deep exome analysis.
Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
Cell type: Mononuclear cell; CL=CL_0000842.
Disease Myelodysplastic syndrome (NCIt: C3247)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_VH25 (MDS-2.13C)
Originate from same individual CVCL_VH20 ! MDS-2.A3
CVCL_VH22 ! N-2.8
CVCL_VH21 ! N-2.12
CVCL_VH24 ! N-2.A2
CVCL_VH23 ! N-2.A11
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=25798938

Markers:
AmelogeninX,Y
CSF1PO11
D2S133816,23
D3S135814,15
D5S81812,13
D7S82010,12
D8S117912,15
D13S31711
D16S53911,13
D19S43313,15
D21S1129,32.2
FGA23
TH016,9.3
TPOX8,10
vWA17

Run an STR similarity search on this cell line
Publications

PubMed=25798938; DOI=10.1038/nbt.3178; PMCID=PMC4464949
Kotini A.G., Chang C.-J., Boussaad I., Delrow J.J., Dolezal E.K., Nagulapally A.B., Perna F., Fishbein G.A., Klimek V.M., Hawkins R.D., Huangfu D.-W., Murry C.E., Graubert T.A., Nimer S.D., Papapetrou E.P.
Functional analysis of a chromosomal deletion associated with myelodysplastic syndromes using isogenic human induced pluripotent stem cells.
Nat. Biotechnol. 33:646-655(2015)

Cross-references
Encyclopedic resources Wikidata; Q54904820
Gene expression databases GEO; GSM1594193
Entry history
Entry creation14-May-2018
Last entry update29-Jun-2023
Version number6