ID   PSADFSV40T373
AC   CVCL_DP39
DR   Wikidata; Q54948443
CC   Part of: Progeria Research Foundation cell lines.
CC   Sequence variation: Mutation; HGNC; 12877; ZMPSTE24; Simple; p.Leu425Pro (c.1274T>C); Zygosity=Homozygous (PRF).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
CC   Miscellaneous: Cell line no longer available.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C34951; Progeria
DI   ORDO; Orphanet_740; Hutchinson-Gilford progeria syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_1Z19 ! PSADFN373
SX   Male
AG   5Y9M
CA   Transformed cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 11
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