ID   PSADFN373
AC   CVCL_1Z19
DR   Wikidata; Q54948436
WW   Provider; PRF; -; https://www.progeriaresearch.org/available-cell-lines/
CC   Part of: Progeria Research Foundation cell lines.
CC   Sequence variation: Mutation; HGNC; HGNC:12877; ZMPSTE24; Simple; p.Leu425Pro (c.1274T>C); Zygosity=Homozygous (PRF).
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)
OI   CVCL_2A01 ! PSALBV341
SX   Male
AG   5Y9M
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 10-04-25; Version: 12
CH   CVCL_DP39 ! PSADFSV40T373
//