ID   WAe001-A-10
AC   CVCL_VE15
SY   H1_RB1ex3_G3; G3
DR   BioSamples; SAMEA5912509
DR   hPSCreg; WAe001-A-10
DR   Wikidata; Q54993537
RX   PubMed=29246572;
CC   From: Universitat Duisburg-Essen; Duisburg; Germany.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; 9884; RB1 (Note=1 of 2 alleles).
CC   Sequence variation: Mutation; HGNC; 9884; RB1; Simple; p.Glu125Valfs*9 (c.374_380del); Zygosity=Heterozygous (PubMed=29246572).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
ST   Source(s): PubMed=29246572
ST   Amelogenin: X,Y
ST   CSF1PO: 12,13
ST   D13S317: 8,11
ST   D16S539: 9,13
ST   D18S51: 17,18
ST   D21S11: 28,32.2
ST   D3S1358: 15
ST   D5S818: 9,11
ST   D7S820: 8,12
ST   D8S1179: 12,13
ST   FGA: 20,24
ST   Penta D: 10,13
ST   Penta E: 10,12
ST   TH01: 10
ST   TPOX: 8,11
ST   vWA: 15,17
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_9771 ! WA01
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 14-05-18; Last updated: 30-01-24; Version: 8
//
RX   PubMed=29246572; DOI=10.1016/j.scr.2017.07.005;
RA   Steenpass L.;
RT   "Generation of two H1 hESC sublines carrying a heterozygous and
RT   homozygous knock-out of RB1.";
RL   Stem Cell Res. 25:270-273(2017).
//