ID   GM05128
AC   CVCL_5N21
DR   CLO; CLO_0025353
DR   Coriell; GM05128
DR   Wikidata; Q54838876
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:2928; DMD; Simple; p.Glu1845Ter (c.5533G>T); ClinVar=VCV000545963; Zygosity=Hemizygous (from familial inference of GM05127).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75482; Duchenne muscular dystrophy
DI   ORDO; Orphanet_98896; Duchenne muscular dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   15Y
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 19-12-24; Version: 9
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