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Cellosaurus TTD11PV (CVCL_RU70)

[Text version]
Cell line name TTD11PV
Synonyms TrichoThioDystrophy 11 PaVia
Accession CVCL_RU70
Resource Identification Initiative To cite this cell line use: TTD11PV (RRID:CVCL_RU70)
Comments From: Istituto di Genetica Biochimica ed Evoluzionistica (IGBE); Pavia; Italy.
Population: Caucasian.
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=9758621).
  • Mutation; HGNC; HGNC:3434; ERCC2; Unexplicit; Ex6del; Zygosity=Heterozygous (PubMed=9758621).
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 5Y
Category Finite cell line
Publications

PubMed=9758621; DOI=10.1086/302063; PMCID=PMC1377495
Botta E., Nardo T., Broughton B.C., Marinoni S., Lehmann A.R., Stefanini M.
Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity.
Am. J. Hum. Genet. 63:1036-1048(1998)

Cross-references
Cell line databases/resources CLO; CLO_0009423
CLDB; cl4550
Encyclopedic resources Wikidata; Q54973258
Entry history
Entry creation05-Mar-2018
Last entry update19-Dec-2024
Version number11