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Cellosaurus MPIMBMi011-A-3 (CVCL_QX64)

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Cell line name MPIMBMi011-A-3
Synonyms F1/PITX2fs/fs-1; PITX2fs/fs-1
Accession CVCL_QX64
Resource Identification Initiative To cite this cell line use: MPIMBMi011-A-3 (RRID:CVCL_QX64)
Comments From: Max Planck Institute for Molecular Biomedicine; Munster; Germany.
Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:9005; PITX2.
Derived from site: In situ; Fetal liver; UBERON=UBERON_0002107.
Disease Atrial fibrillation (NCIt: C50466)
Familial atrial fibrillation (ORDO: Orphanet_334)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_QX63 (MPIMBMi011-A)
Sex of cell Male
Age at sampling Fetus
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=28677534

Markers:
AmelogeninX,Y
CSF1PO11,14
D1S165612,14
D2S133818,19
D3S135814,17
D5S81811,12
D6S104312
D7S82011,12
D8S117912,14
D12S39117.3,19
D13S31712
D16S53911,12
D18S5112,18
D19S43313,14
D21S1127,30
FGA23,25
Penta D9,12
Penta E12,16
TH016,9
TPOX8,11
vWA17

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Publications

PubMed=28677534; DOI=10.1016/j.scr.2017.03.015
Maike Marczenke, Jakob Fell, Ilaria Piccini, Albrecht Ropke, Guiscard Seebohm, Boris Greber;
Generation and cardiac subtype-specific differentiation of PITX2-deficient human iPS cell lines for exploring familial atrial fibrillation.
Stem Cell Res. 21:26-28(2017)

Cross-references
Encyclopedic resources Wikidata; Q54906459
Entry history
Entry creation15-Nov-2017
Last entry update19-Dec-2024
Version number7