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Cellosaurus PSFDFN388 (CVCL_YU45)

[Text version]
Cell line name PSFDFN388
Accession CVCL_YU45
Resource Identification Initiative To cite this cell line use: PSFDFN388 (RRID:CVCL_YU45)
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 Male
Age at sampling 38Y1M
Category Finite cell line
STR profile Source(s): PubMed=27920058

Markers:
AmelogeninX,Y
CSF1PO10,13
D2S133824
D3S135815,16
D5S81811,13
D7S82011
D8S117911,12
D13S31712,13
D16S53911,13
D18S5115,18
D19S43315
D21S1130,33.2
FGA20,21
TH019,9.3
TPOX8
vWA14,18

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; Q98128677
Entry history
Entry creation12-Mar-2020
Last entry update29-Jun-2023
Version number5