ID   GM26579
AC   CVCL_LH33
DR   Coriell; GM26579
DR   Wikidata; Q54854100
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:30171; HSPB8; Simple; p.Pro173Serfs*43 (c.515dupC); ClinVar=VCV000986227; Zygosity=Heterozygous (Coriell=GM26579).
CC   Derived from site: In situ; Flank, skin; UBERON=UBERON_8480023.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C122663; Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1
DI   ORDO; Orphanet_206662; Inclusion myopathy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   66Y
CA   Finite cell line
DT   Created: 15-11-17; Last updated: 19-12-24; Version: 13
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