ID   iPSC-CGD3
AC   CVCL_V184
DR   Wikidata; Q54898222
RX   PubMed=22311747;
CC   Sequence variation: Mutation; HGNC; HGNC:2578; CYBB; Unexplicit; Ex1-3del; Zygosity=Hemizygous (PubMed=22311747).
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): PubMed=22311747
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D13S317: 9,11
ST   D16S539: 9,11
ST   D18S51: 10,16
ST   D21S11: 28
ST   D3S1358: 15,17
ST   D5S818: 12,13
ST   D7S820: 10,11
ST   D8S1179: 14,15
ST   FGA: 21,24
ST   Penta D: 13
ST   Penta E: 11,14
ST   TH01: 8
ST   TPOX: 8
ST   vWA: 17,18
DI   NCIt; C154315; X-linked chronic granulomatous disease
DI   ORDO; Orphanet_379; Chronic granulomatous disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 16-04-14; Last updated: 19-12-24; Version: 11
//
RX   PubMed=22311747; DOI=10.1002/stem.1053; PMCID=PMC3593166;
RA   Jiang Y., Cowley S.A., Siler U., Melguizo-Sanchis D., Tilgner K.,
RA   Browne C., Dewilton A., Przyborski S.A., Saretzki G., James W.S.,
RA   Seger R.A., Reichenbach J., Lako M., Armstrong L.;
RT   "Derivation and functional analysis of patient-specific induced
RT   pluripotent stem cells as an in vitro model of chronic granulomatous
RT   disease.";
RL   Stem Cells 30:599-611(2012).
//