ID   HEK293 FUS KO
AC   CVCL_A0TJ
SY   HEK293 FUS knockout; FUS KO HEK293
DR   Millipore; SCC292
DR   Wikidata; Q108820443
RX   PubMed=30206235;
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; 4010; FUS.
CC   Transformant: NCBI_TaxID; 28285; Adenovirus 5.
CC   Derived from site: In situ; Fetal kidney; UBERON=UBERON_0002113.
ST   Source(s): Millipore=SCC292
ST   Amelogenin: X
ST   CSF1PO: 12
ST   D13S317: 12
ST   D16S539: 9,10,13
ST   D18S51: 17,18
ST   D21S11: 28,30.2
ST   D3S1358: 15,17
ST   D5S818: 8
ST   D7S820: 11,12
ST   D8S1179: 12,14
ST   FGA: 23
ST   Penta D: 9
ST   Penta E: 7,15
ST   TH01: 9.3
ST   TPOX: 11
ST   vWA: 16,19
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0045 ! HEK293
SX   Female
AG   Fetus
CA   Transformed cell line
DT   Created: 23-09-21; Last updated: 02-05-24; Version: 6
//
RX   PubMed=30206235; DOI=10.1038/s41467-018-06111-6;
RA   Wang H.-B., Guo W.-T., Mitra J., Hegde P.M., Vandoorne T.,
RA   Eckelmann B.J., Mitra S., Tomkinson A.E., Van Den Bosch L., Hegde M.L.;
RT   "Mutant FUS causes DNA ligation defects to inhibit oxidative damage
RT   repair in amyotrophic lateral sclerosis.";
RL   Nat. Commun. 9:3683.1-3683.18(2018).
//