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Cellosaurus TRNDi012-E (CVCL_A0LN)

[Text version]

Cell line name TRNDi012-E
Synonyms HT216E
Accession CVCL_A0LN
Resource Identification Initiative To cite this cell line use: TRNDi012-E (RRID:CVCL_A0LN)
Comments From: NIH-NCATS-TRND Branch; Rockville; USA.
Population: Caucasian.
Derived from sampling site: Arm; skin.
Sequence variations Mutation; HGNC; 171; ACVR1; Simple; p.Arg206His (c.617G>A); ClinVar=VCV000018309; Zygosity=Heterozygous (from autologous cell line).
Disease Fibrodysplasia ossificans progressiva (NCIt: C3040)
Fibrodysplasia ossificans progressiva (ORDO: Orphanet_337)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_W541 (GM00513)
Sex of cell Female
Age at sampling 16Y
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; TRNDi012-E
Encyclopedic resources Wikidata; Q108821388
Entry history
Entry creation23-Sep-2021
Last entry update16-Dec-2021
Version number2