Cellosaurus cell line GM16877 (CVCL

Cellosaurus GM16877 (CVCL_RG79)

Cross-references
Cell line name	GM16877
Synonyms	XPTTD268BE
Accession	CVCL_RG79
Resource Identification Initiative	To cite this cell line use: GM16877 (RRID:CVCL_RG79)
Comments	Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:3434; ERCC2; Simple; p.Arg112His (c.335G>A); ClinVar=VCV000016784; Zygosity=Heterozygous (PubMed=18470933). Mutation; HGNC; HGNC:3434; ERCC2; Simple; p.Cys663Arg (c.1987T>C); dbSNP=rs770367713; Zygosity=Heterozygous (PubMed=18470933).
Disease	Trichothiodystrophy 1, photosensitive (NCIt: C156433) Xeroderma pigmentosum, complementation group D (NCIt: C3967) Trichothiodystrophy (ORDO: Orphanet_33364) Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	18Y
Category	Finite cell line
Publications	PubMed=18470933; DOI=10.1002/humu.20768; PMCID=PMC3477783 Jennifer Boyle, Takahiro Ueda, Kyu-Seon Oh, Kyoko Imoto, Deborah Tamura, Jared Jagdeo, Sikandar G. Khan, Carine Nadem, John Joseph DiGiovanna, Kenneth H. Kraemer; Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy. Hum. Mutat. 29:1194-1208(2008)
Cell line collections (Providers)	Coriell; GM16877 - Discontinued
Encyclopedic resources	Wikidata; Q54848794
Entry history
Entry creation	05-Mar-2018
Last entry update	19-Dec-2024
Version number	13