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Cellosaurus TRNDi009-B (CVCL_WU19)

[Text version]
Cell line name TRNDi009-B
Synonyms HT220B
Accession CVCL_WU19
Resource Identification Initiative To cite this cell line use: TRNDi009-B (RRID:CVCL_WU19)
Comments From: NIH-NCATS-TRND Branch; Rockville; USA.
Population: Caucasian.
Derived from site: In situ; Fetus; UBERON=UBERON_0000323.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; HGNC:11120; SMPD1; Simple; p.Leu304Pro (c.911T>C) (L302P); ClinVar=VCV000002989; Zygosity=Heterozygous (from parent cell line).
Disease Niemann-Pick disease, type A (NCIt: C126561)
Niemann-Pick disease type A (ORDO: Orphanet_77292)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_7379 (GM03252)
Sex of cell Female
Age at sampling 21FW
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; TRNDi009-B
Encyclopedic resources Wikidata; Q98133600
Entry history
Entry creation05-Jul-2019
Last entry update19-Dec-2024
Version number9