ID   GM16891
AC   CVCL_U715
SY   HG1824
DR   CLO; CLO_0018105
DR   Coriell; GM16891
DR   GEO; GSM476015
DR   GEO; GSM1316993
DR   GEO; GSM1317032
DR   Wikidata; Q54848804
RX   PubMed=17407155;
RX   PubMed=19966276;
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:1058; BLM; Simple; p.Gln645Ter (c.1933C>T); ClinVar=VCV000454091; Zygosity=Homozygous (PubMed=17407155; Coriell=GM16891).
CC   Omics: miRNA expression profiling.
CC   Omics: Transcriptome analysis by microarray.
CC   Donor information: From Bloom Syndrome Registry patient 169 (BSR169).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C2903; Bloom syndrome
DI   ORDO; Orphanet_125; Bloom syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   30Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 19-12-24; Version: 16
//
RX   PubMed=17407155; DOI=10.1002/humu.20501;
RA   German J.L. 3rd, Sanz M.M., Ciocci S., Ye T.-Z., Ellis N.A.;
RT   "Syndrome-causing mutations of the BLM gene in persons in the Bloom's
RT   Syndrome Registry.";
RL   Hum. Mutat. 28:743-753(2007).
//
RX   PubMed=19966276; DOI=10.1093/nar/gkp1103; PMCID=PMC2831322;
RA   Johnson J.E., Cao K., Ryvkin P., Wang L.-S., Johnson F.B.;
RT   "Altered gene expression in the Werner and Bloom syndromes is
RT   associated with sequences having G-quadruplex forming potential.";
RL   Nucleic Acids Res. 38:1114-1122(2010).
//