ID   GM21889
AC   CVCL_U542
DR   Coriell; GM21889
DR   Wikidata; Q54852210
RX   PubMed=23665875;
RX   PubMed=24816254;
CC   Population: African American.
CC   Omics: Variations; CNV analysis.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C75463; Prader-Willi syndrome
DI   ORDO; Orphanet_739; Prader-Willi syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   8Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 10-04-25; Version: 11
//
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).
//
RX   PubMed=24816254; DOI=10.1038/ng.2968;
RA   Stelzer Y., Sagi I., Yanuka O., Eiges R., Benvenisty N.;
RT   "The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an
RT   induced pluripotent stem cell model of Prader-Willi syndrome.";
RL   Nat. Genet. 46:551-557(2014).
//