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Cellosaurus PSMDFN387 (CVCL_YU44)

[Text version]
Cell line name PSMDFN387
Accession CVCL_YU44
Resource Identification Initiative To cite this cell line use: PSMDFN387 (RRID:CVCL_YU44)
Comments Part of: Progeria Research Foundation cell lines.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 36Y5M
Category Finite cell line
STR profile Source(s): PubMed=27920058

Markers:
AmelogeninX
CSF1PO10,11
D2S133817,24
D3S135814,15
D5S81811,13
D7S8208,11
D8S117914
D13S31711,12
D16S53911,12
D18S5112,15
D19S43314
D21S1128,31.2
FGA21,23
TH016,9.3
TPOX11,12
vWA16,17

Run an STR similarity search on this cell line
Web pages https://www.progeriaresearch.org/available-cell-lines/
Publications

PubMed=27920058; DOI=10.1136/jmedgenet-2016-104295
Bar D.Z., Arlt M.F., Brazier J.F., Norris W.E., Campbell S.E., Chines P.S., Larrieu D., Jackson S.P., Collins F.S., Glover T.W., Gordon L.B.
A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome.
J. Med. Genet. 54:212-216(2017)

Cross-references
Encyclopedic resources Wikidata; Q98128681
Entry history
Entry creation12-Mar-2020
Last entry update29-Jun-2023
Version number5