ID   F09152
AC   CVCL_ZD02
SY   CS52; ALS52
DR   CLO; CLO_0037419
DR   LINCS_LDP; LPC-1020
DR   Wikidata; Q98125978
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:28337; C9orf72; Repeat_expansion; c.-45+163GGGGCC[>24] (GGGGCC repeat expansion); ClinVar=VCV000031151; Zygosity=Unspecified (from child cell line ND50075).
CC   Caution: Indicated as originating from a 60 year old male donor in LINCS.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C168756; Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
DI   ORDO; Orphanet_803; Amyotrophic lateral sclerosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   49Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 19-12-24; Version: 10
//