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Cellosaurus TRNDi003-B (CVCL_UL13)

[Text version]
Cell line name TRNDi003-B
Synonyms HT215B
Accession CVCL_UL13
Resource Identification Initiative To cite this cell line use: TRNDi003-B (RRID:CVCL_UL13)
Comments From: NIH-NCATS-TRND Branch; Rockville; USA.
Population: African; Somali.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 9644; PTPN11; Simple; p.Gln510Pro (c.1529A>C); ClinVar=VCV000013344; Zygosity=Heterozygous (from autologous cell line TRNDi003-A).
Disease Noonan syndrome (NCIt: C34854)
Noonan syndrome (ORDO: Orphanet_648)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UL12 ! TRNDi003-A
Sex of cell Female
Age at sampling 13Y
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; TRNDi003-B
Encyclopedic resources Wikidata; Q98133580
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number8