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Cellosaurus AP7P (CVCL_J287)

[Text version]
Cell line name AP7P
Synonyms AP07P
Accession CVCL_J287
Resource Identification Initiative To cite this cell line use: AP7P (RRID:CVCL_J287)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:3582; FANCA; Simple; c.2152_2778del (Ex24-28del); Zygosity=Heterozygous (DOI=10.1007/0-387-33776-8_11; PubMed=10090479).
  • Mutation; HGNC; HGNC:3582; FANCA; Simple; p.Ser849Phefs*40 (c.2546delC); ClinVar=VCV000408166; Zygosity=Heterozygous (DOI=10.1007/0-387-33776-8_11; PubMed=10090479).
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_L454 (AP7P(SVT))
Sex of cell Female
Age at sampling 7Y
Category Finite cell line
STR profile Source(s): JCRB=JCRB3011

Markers:
AmelogeninX
CSF1PO9,10
D5S81810
D7S82010,12
D13S3178,9
D16S53910,11
TH019,10
TPOX8,11
vWA14,17

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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)

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

Cross-references
Cell line collections (Providers) JCRB; JCRB3011
JCRB; KURB1401 - Discontinued
Biological sample resources BioSample; SAMN03472407
Encyclopedic resources Wikidata; Q54750300
Entry history
Entry creation11-Feb-2013
Last entry update19-Dec-2024
Version number19