Cellosaurus cell line XP18OS (CVCL

Cellosaurus XP18OS (CVCL_JH24)

[Text version]

Cell line name

XP18OS

Synonyms

Xeroderma Pigmentosum 18 OSaka

Accession

CVCL_JH24

Resource Identification Initiative

To cite this cell line use: XP18OS (RRID:CVCL_JH24)

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:12814; XPA; Simple; p.Tyr116Ter (c.348T>A); ClinVar=VCV000000997; Zygosity=Homozygous (PubMed=7947212).

Disease

Xeroderma pigmentosum, complementation group A (NCIt: C3965)
Xeroderma pigmentosum (ORDO: Orphanet_910)

Species of origin

Homo sapiens (Human) (NCBI Taxonomy: 9606)

Sex of cell

Female

Age at sampling

Category

Finite cell line

STR profile

Source(s): JCRB=JCRB3027

Markers:

Amelogenin	X
CSF1PO	10,12
D5S818	12,13
D7S820	11
D13S317	8,9
D16S539	9,13
TH01	9
TPOX	8,9
vWA	14,18

Publications

PubMed=832273
Takebe H., Miki Y., Kozuka T., Furuyama J.-i., Tanaka K., Sasaki M.S., Fujiwara Y., Akiba H.
DNA repair characteristics and skin cancers of xeroderma pigmentosum patients in Japan.
Cancer Res. 37:490-495(1977)

PubMed=7947212; DOI=10.1111/j.1365-2133.1994.tb08562.x
Maeda T., Sato K., Minami H., Taguchi H., Yoshikawa K.
Severe neurological abnormalities associated with a mutation in the zinc-finger domain in a group A xeroderma pigmentosum patient.
Br. J. Dermatol. 131:566-570(1994)

Cross-references

Cell line collections (Providers)

JCRB; JCRB3027
JCRB; KURB1234 - Discontinued
JCRB; KURB1330 - Discontinued

Encyclopedic resources

Wikidata; Q54994894

Entry history

Entry creation

15-May-2017

Last entry update

19-Dec-2024

Version number