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Cellosaurus 1321N1-MFSD1-KO-c5 (CVCL_D4EC)

[Text version]
Cell line name 1321N1-MFSD1-KO-c5
Synonyms CE0578-Q
Accession CVCL_D4EC
Resource Identification Initiative To cite this cell line use: 1321N1-MFSD1-KO-c5 (RRID:CVCL_D4EC)
Comments Problematic cell line: Contaminated. Ancestral cell line (U-118MG) has been shown to be a U-138MG derivative.
Part of: Research Empowerment on Solute Carriers (RESOLUTE) KO cell line panel.
Population: Caucasian.
Knockout cell: Method=CRISPR/Cas9; HGNC; 25874; MFSD1.
Derived from site: In situ; Brain; UBERON=UBERON_0000955.
Sequence variations
  • Mutation; 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; 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://re-solute.eu/resources/reagents
Cross-references
Encyclopedic resources Wikidata; Q127378570
Entry history
Entry creation30-Jan-2024
Last entry update10-Sep-2024
Version number2