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Cellosaurus FA18JTO hTERT (CVCL_D253)

[Text version]
Cell line name FA18JTO hTERT
Accession CVCL_D253
Resource Identification Initiative To cite this cell line use: FA18JTO hTERT (RRID:CVCL_D253)
Comments Population: Japanese.
Transfected with: HGNC; 11730; TERT.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 3582; FANCA; Simple; c.1811delT; Zygosity=Heterozygous (from parent cell line).
  • Mutation; HGNC; 3582; FANCA; Simple; p.Ser849Phefs*40 (c.2546delC); ClinVar=VCV000408166; Zygosity=Heterozygous (from parent cell line).
Disease Fanconi anemia, complementation group A (NCIt: C125702)
Fanconi anemia (ORDO: Orphanet_84)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_2895 (FA18JTO)
Sex of cell Male
Age at sampling Age unspecified
Category Telomerase immortalized cell line
STR profile Source(s): JCRB

Markers:
AmelogeninX,Y
CSF1PO10,14
D5S81811,13
D7S82011
D13S3178,10
D16S53911
TH016,9
TPOX11
vWA16,18

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Cross-references
Cell line collections (Providers) JCRB; JCRB3007
JCRB; KURB1389 - Discontinued
Encyclopedic resources Wikidata; Q54833175
Entry history
Entry creation22-Oct-2012
Last entry update29-Jun-2023
Version number16