ID   TTD15PV
AC   CVCL_ZT13
SY   TrichoThioDystrophy 15 PaVia
DR   Wikidata; Q98133653
RX   PubMed=9758621;
CC   From: Istituto di Genetica Biochimica ed Evoluzionistica (IGBE); Pavia; Italy.
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:3434; ERCC2; Simple; p.Cys259Tyr (c.776G>A); ClinVar=VCV000329522; Zygosity=Heterozygous (PubMed=9758621).
CC   Sequence variation: Mutation; HGNC; HGNC:3434; ERCC2; Simple; p.Arg722Trp (c.2164C>T); ClinVar=VCV000016792; Zygosity=Heterozygous (PubMed=9758621).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C156433; Trichothiodystrophy 1, photosensitive
DI   ORDO; Orphanet_33364; Trichothiodystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   3-4Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 19-12-24; Version: 8
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RX   PubMed=9758621; DOI=10.1086/302063; PMCID=PMC1377495;
RA   Botta E., Nardo T., Broughton B.C., Marinoni S., Lehmann A.R.,
RA   Stefanini M.;
RT   "Analysis of mutations in the XPD gene in Italian patients with
RT   trichothiodystrophy: site of mutation correlates with repair
RT   deficiency, but gene dosage appears to determine clinical severity.";
RL   Am. J. Hum. Genet. 63:1036-1048(1998).
//