ID   GM10490
AC   CVCL_N146
SY   GM10490A; GM17170
DR   CLO; CLO_0014022
DR   CLO; CLO_0024254
DR   BioSample; SAMN00800043
DR   Coriell; GM10490
DR   Coriell; GM17170
DR   GEO; GSM569696
DR   GEO; GSM596234
DR   GEO; GSM597029
DR   GEO; GSM924680
DR   IPD-IMGT/HLA; 19225
DR   Wikidata; Q54844490
RX   CelloPub=CLPUB00447;
CC   Part of: Human variation panel.
CC   Population: African American.
CC   HLA typing: A*03:CVAB,34:02; B*07:CZZS,42:01; C*07:WCP,17:MN; DRB1*03:02,15:03 (IPD-IMGT/HLA=19225).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Omics: Genomics; DNA methylation analysis.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C35261; Congenital adrenal gland hypoplasia
DI   ORDO; Orphanet_595337; Adrenal hypoplasia congenita
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_N145 ! GM09964
SX   Female
AG   17Y
CA   Transformed cell line
DT   Created: 05-11-13; Last updated: 10-04-25; Version: 17
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992).
//