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Cellosaurus HT149B (CVCL_UD80)

[Text version]
Cell line name HT149B
Accession CVCL_UD80
Resource Identification Initiative To cite this cell line use: HT149B (RRID:CVCL_UD80)
Comments From: NIH-NCATS-TRND Branch; Rockville; USA.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Wolman disease (NCIt: C61271)
Wolman disease (ORDO: Orphanet_75233)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_8B12 (GM11851)
Sex of cell Female
Age at sampling 4M
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=28659158

Markers:
AmelogeninX
CSF1PO10,12
D3S135814,16
D5S81811,12
D7S82010,12
D8S117913
D13S3179,12
D16S53911,13
D18S5114,15
D21S1128,29
FGA21
Penta D9,11
Penta E11,13
TH016,7
TPOX8
vWA17

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Publications

PubMed=28659158; DOI=10.1186/s13023-017-0670-9; PMCID=PMC5490176
Francis Aguisanda, Charles D. Yeh, Catherine Z. Chen, Rong Li, Jeanette K. Beers, Ji-Zhong Zou, Natasha Thorne, Wei Zheng;
Neural stem cells for disease modeling of Wolman disease and evaluation of therapeutics.
Orphanet J. Rare Dis. 12:120.1-120.13(2017)

Cross-references
Encyclopedic resources Wikidata; Q94305139
Entry history
Entry creation13-Nov-2018
Last entry update29-Jun-2023
Version number8