ID   MPIMBMi011-A-3
AC   CVCL_QX64
SY   F1/PITX2fs/fs-1; PITX2fs/fs-1
DR   Wikidata; Q54906459
RX   PubMed=28677534;
CC   From: Max Planck Institute for Molecular Biomedicine; Munster; Germany.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:9005; PITX2.
CC   Derived from site: In situ; Fetal liver; UBERON=UBERON_0002107.
ST   Source(s): PubMed=28677534
ST   Amelogenin: X,Y
ST   CSF1PO: 11,14
ST   D12S391: 17.3,19
ST   D13S317: 12
ST   D16S539: 11,12
ST   D18S51: 12,18
ST   D19S433: 13,14
ST   D1S1656: 12,14
ST   D21S11: 27,30
ST   D2S1338: 18,19
ST   D3S1358: 14,17
ST   D5S818: 11,12
ST   D6S1043: 12
ST   D7S820: 11,12
ST   D8S1179: 12,14
ST   FGA: 23,25
ST   Penta D: 9,12
ST   Penta E: 12,16
ST   TH01: 6,9
ST   TPOX: 8,11
ST   vWA: 17
DI   NCIt; C50466; Atrial fibrillation
DI   ORDO; Orphanet_334; Familial atrial fibrillation
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_QX63 ! MPIMBMi011-A
SX   Male
AG   Fetus
CA   Induced pluripotent stem cell
DT   Created: 15-11-17; Last updated: 19-12-24; Version: 7
//
RX   PubMed=28677534; DOI=10.1016/j.scr.2017.03.015;
RA   Marczenke, Maike
RA   Fell, Jakob
RA   Piccini, Ilaria
RA   Ropke, Albrecht
RA   Seebohm, Guiscard
RA   Greber, Boris
RT   "Generation and cardiac subtype-specific differentiation of
RT   PITX2-deficient human iPS cell lines for exploring familial atrial
RT   fibrillation.";
RL   Stem Cell Res. 21:26-28(2017).
//