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Cellosaurus AP38P(SVT) (CVCL_JG64)

[Text version]
Cell line name AP38P(SVT)
Accession CVCL_JG64
Resource Identification Initiative To cite this cell line use: AP38P(SVT) (RRID:CVCL_JG64)
Comments Population: Japanese.
Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) [Note=pSVori-].
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 3582; FANCA; Simple; p.Ser849Phefs*40 (c.2546delC); ClinVar=VCV000408166; Zygosity=Homozygous (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_JG62 (AP38P)
Sex of cell Female
Age at sampling 9Y
Category Transformed cell line
STR profile Source(s): JCRB

Markers:
AmelogeninX
CSF1PO12,15
D5S8189,11
D7S82010,11
D13S3179
D16S53911,14
TH016,9
TPOX8,11
vWA15,17

Run an STR similarity search on this cell line
Cross-references
Cell line collections (Providers) JCRB; JCRB3026
JCRB; KURB1432 - Discontinued
Encyclopedic resources Wikidata; Q54750237
Entry history
Entry creation15-May-2017
Last entry update05-Oct-2023
Version number11