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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

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Web pages Provider; PRF; -; https://www.progeriaresearch.org/available-cell-lines/
Publications

PubMed=27920058; DOI=10.1136/jmedgenet-2016-104295; PMCID=PMC5384422
Daniel Z. Bar, Martin F. Arlt, Joan F. Brazier, Wendy E. Norris, Susan E. Campbell, Peter S. Chines, Delphine Larrieu, Stephen Philip Jackson, Francis Sellers Collins, Thomas W. Glover, Leslie Beth Gordon;
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 update10-Apr-2025
Version number6