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Cellosaurus 1321N1/P2Y11 (CVCL_H356)

[Text version]
Cell line name 1321N1/P2Y11
Accession CVCL_H356
Resource Identification Initiative To cite this cell line use: 1321N1/P2Y11 (RRID:CVCL_H356)
Comments Problematic cell line: Contaminated. Ancestral cell line (U-118MG) has been shown to be a U-138MG derivative.
Population: Caucasian.
Genetic integration: Method=Transfection; Gene=HGNC; HGNC:8540; P2RY11.
Derived from site: In situ; Brain; UBERON=UBERON_0000955.
Sequence variations
  • Mutation; HGNC; HGNC:9588; PTEN; Simple; c.1026+1G>T (IVS8+1G>T); ClinVar=VCV000635377; Zygosity=Homozygous; Note=Splice donor mutation (from parent cell line).
  • Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg213Gln (c.638G>A); ClinVar=VCV000135359; Zygosity=Homozygous (from parent cell line).
Disease Astrocytoma (NCIt: C60781)
Astrocytoma (ORDO: Orphanet_94)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_0110 (1321N1)
Sex of cell Male
Age at sampling 47Y
Category Cancer cell line
Web pages https://www.genscript.com/molecule/M00298-P2Y11.html
Cross-references
Cell line databases/resources cancercelllines; CVCL_H356
Encyclopedic resources Wikidata; Q54581492
Entry history
Entry creation11-Feb-2013
Last entry update19-Dec-2024
Version number20