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Cellosaurus AP78P (CVCL_JH20)

[Text version]
Cell line name AP78P
Accession CVCL_JH20
Resource Identification Initiative To cite this cell line use: AP78P (RRID:CVCL_JH20)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Fanconi anemia, complementation group A (NCIt: C125702)
Fanconi anemia (ORDO: Orphanet_84)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 1Y
Category Finite cell line
STR profile Source(s): JCRB=JCRB3033

Markers:
AmelogeninX,Y
CSF1PO10,12
D5S81810,11
D7S82010
D13S3178,11
D16S53911,12
TH016,9
TPOX8,10
vWA14,18

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Publications

DOI=10.1007/0-387-33776-8_11
Tachibana A.
Mutational analyses of Fanconi anemia genes in Japanese patients.
(In) Molecular mechanisms of Fanconi anemia; Ahmad S.I., Kirk S.H. (eds.); pp.103-114; Springer; New York (2006)

Cross-references
Cell line collections (Providers) JCRB; JCRB3033
JCRB; KURB1570 - Discontinued
Encyclopedic resources Wikidata; Q54750298
Entry history
Entry creation15-May-2017
Last entry update02-May-2024
Version number11