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Cellosaurus HPS1097 (CVCL_A3SX)

[Text version]
Cell line name HPS1097
Synonyms BRCi013-B
Accession CVCL_A3SX
Resource Identification Initiative To cite this cell line use: HPS1097 (RRID:CVCL_A3SX)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:61; ABCD1; Simple; p.Leu670Phefs*63 (c.2010_2014delinsTAT); Zygosity=Hemizygous (from autologous cell line HPS1096).
Disease Adrenoleukodystrophy (NCIt: C61252)
X-linked cerebral adrenoleukodystrophy (ORDO: Orphanet_139396)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UP34 ! HPS1096
CVCL_A3SY ! HPS1098
CVCL_A3SZ ! HPS1099
CVCL_A3TA ! HPS1100
CVCL_A3TB ! HPS1101
Sex of cell Male
Age at sampling 10-19Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS1097
Cell line databases/resources hPSCreg; BRCi013-B
Encyclopedic resources Wikidata; Q105507780
Entry history
Entry creation12-Jan-2021
Last entry update19-Dec-2024
Version number7