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Cellosaurus AP25P (CVCL_JG72)

[Text version]
Cell line name AP25P
Accession CVCL_JG72
Resource Identification Initiative To cite this cell line use: AP25P (RRID:CVCL_JG72)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Fanconi anemia, complementation group A (NCIt: C125702)
Fanconi anemia (ORDO: Orphanet_84)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_XD37 (AP25P(SVT))
Sex of cell Male
Age at sampling 3Y
Category Finite cell line
Publications

PubMed=10090479; DOI=10.1002/(SICI)1098-1004(1999)13:3<237::AID-HUMU8>3.0.CO;2-F
Tachibana A., Kato T., Ejima Y., Yamada T., Shimizu T., Yang L.-C., Tsunematsu Y., Sasaki M.S.
The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability.
Hum. Mutat. 13:237-244(1999)

Cross-references
Cell line collections (Providers) JCRB; KURB1538
Encyclopedic resources Wikidata; Q54750213
Entry history
Entry creation15-May-2017
Last entry update29-Jun-2023
Version number8