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Cellosaurus N-2.12 (CVCL_VH21)

[Text version]
Cell line name N-2.12
Accession CVCL_VH21
Resource Identification Initiative To cite this cell line use: N-2.12 (RRID:CVCL_VH21)
Comments Omics: Genomics; Whole exome sequencing.
Derived from site: In situ; Bone marrow; UBERON=UBERON_0002371.
Cell type: Mononuclear cell of bone marrow; CL=CL_0010004.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_VH19 ! MDS-2.13
CVCL_VH20 ! MDS-2.A3
CVCL_VH22 ! N-2.8
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
D18S5114,16
D19S43313,15
D21S1129,32.2
FGA23
TH016,9.3
TPOX8,10
vWA17

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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; Q54907274
Entry history
Entry creation14-May-2018
Last entry update10-Apr-2025
Version number7