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Cellosaurus S1120-03 iPS #1 (CVCL_A2ZL)

[Text version]
Cell line name S1120-03 iPS #1
Synonyms S1120-03#1; i1120-03#1
Accession CVCL_A2ZL
Resource Identification Initiative To cite this cell line use: S1120-03 iPS #1 (RRID:CVCL_A2ZL)
Comments Omics: Genomics; Whole genome sequencing.
Omics: Transcriptomics; RNAseq.
Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Autism spectrum disorder (NCIt: C88412)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A2ZG (S1120-03 fibroblast)
Sex of cell Male
Age at sampling 10Y
Category Induced pluripotent stem cell
Publications

PubMed=26186191; DOI=10.1016/j.cell.2015.06.034; PMCID=PMC4519016
Mariani J., Coppola G., Zhang P., Abyzov A., Provini L., Tomasini L., Amenduni M., Szekely A., Palejev D., Wilson M., Gerstein M.B., Grigorenko E.L., Chawarska K., Pelphrey K.A., Howe J.R., Vaccarino F.M.
FOXG1-dependent dysregulation of GABA/glutamate neuron differentiation in autism spectrum disorders.
Cell 162:375-390(2015)

PubMed=28235832; DOI=10.1101/gr.215517.116; PMCID=PMC5378170
Abyzov A., Tomasini L., Zhou B., Vasmatzis N., Coppola G., Amenduni M., Pattni R., Wilson M., Gerstein M.B., Weissman S.M., Urban A.E., Vaccarino F.M.
One thousand somatic SNVs per skin fibroblast cell set baseline of mosaic mutational load with patterns that suggest proliferative origin.
Genome Res. 27:512-523(2017)

Cross-references
Cell line databases/resources SKIP; SKIP001211
Encyclopedic resources Wikidata; Q105510869
Entry history
Entry creation12-Jan-2021
Last entry update10-Apr-2025
Version number6