ID   PSADFN414
AC   CVCL_1Z26
DR   Wikidata; Q54948439
CC   Part of: Progeria Research Foundation cell lines.
CC   Sequence variation: Mutation; HGNC; HGNC:6636; LMNA; Simple; p.Cys588Arg (c.1762T>C); ClinVar=VCV000066865; Zygosity=Heterozygous (PRF).
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)
OI   CVCL_1Z25 ! PSADFN412
SX   Male
AG   12Y8M
CA   Finite cell line
DT   Created: 22-09-15; Last updated: 19-12-24; Version: 12
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