ID   GM23125
AC   CVCL_5S75
SY   801-011 LCL
DR   Coriell; GM23125
DR   Wikidata; Q54852899
RX   PubMed=23495136;
RX   PubMed=23665875;
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Omics: Variations; CNV analysis.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C88412; Autism spectrum disorder
DI   NCIt; C126692; Chromosome 15q11-q13 duplication syndrome
DI   ORDO; Orphanet_238446; 15q11q13 microduplication syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   6Y
CA   Transformed cell line
DT   Created: 23-02-16; Last updated: 10-04-25; Version: 9
//
RX   PubMed=23495136; DOI=10.1002/aur.1284; PMCID=PMC3884762;
RA   Urraca N., Cleary J., Brewer V., Pivnick E.K., McVicar K.,
RA   Thibert R.L., Schanen N.C., Esmer C., Lamport D., Reiter L.T.;
RT   "The interstitial duplication 15q11.2-q13 syndrome includes autism,
RT   mild facial anomalies and a characteristic EEG signature.";
RL   Autism Res. 6:268-279(2013).
//
RX   PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242;
RA   Tang Z.-Y., Berlin D.S., Toji L.H., Toruner G.A., Beiswanger C.M.,
RA   Kulkarni S., Martin C.L., Emanuel B.S., Christman M., Gerry N.P.;
RT   "A dynamic database of microarray-characterized cell lines with
RT   various cytogenetic and genomic backgrounds.";
RL   G3 (Bethesda) 3:1143-1149(2013).
//