ID   S1120-03 iPS #5
AC   CVCL_A2ZN
SY   S1120-03#5; i1120-03#5
DR   SKIP; SKIP001213
DR   Wikidata; Q105510883
RX   PubMed=26186191;
RX   PubMed=28235832;
CC   Omics: Genome sequenced.
CC   Omics: Transcriptome analysis by RNAseq.
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C88412; Autism spectrum disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_A2ZG ! S1120-03 fibroblast
SX   Male
AG   10Y
CA   Induced pluripotent stem cell
DT   Created: 12-01-21; Last updated: 29-06-23; Version: 5
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RX   PubMed=26186191; DOI=10.1016/j.cell.2015.06.034; PMCID=PMC4519016;
RA   Mariani J., Coppola G., Zhang P., Abyzov A., Provini L., Tomasini L.,
RA   Amenduni M., Szekely A., Palejev D., Wilson M., Gerstein M.B.,
RA   Grigorenko E.L., Chawarska K., Pelphrey K.A., Howe J.R.,
RA   Vaccarino F.M.;
RT   "FOXG1-dependent dysregulation of GABA/glutamate neuron
RT   differentiation in autism spectrum disorders.";
RL   Cell 162:375-390(2015).
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RX   PubMed=28235832; DOI=10.1101/gr.215517.116; PMCID=PMC5378170;
RA   Abyzov A., Tomasini L., Zhou B., Vasmatzis N., Coppola G.,
RA   Amenduni M., Pattni R., Wilson M., Gerstein M.B., Weissman S.M.,
RA   Urban A.E., Vaccarino F.M.;
RT   "One thousand somatic SNVs per skin fibroblast cell set baseline of
RT   mosaic mutational load with patterns that suggest proliferative
RT   origin.";
RL   Genome Res. 27:512-523(2017).
//