Cellosaurus cell line WS77-c5 (CVCL

Cross-references
Cell line name	WS77-c5
Accession	CVCL_RJ00
Resource Identification Initiative	To cite this cell line use: WS77-c5 (RRID:CVCL_RJ00)
Comments	Omics: Transcriptomics; RNAseq. Omics: Variations; SNP array analysis. Derived from site: In situ; Tooth, dental pulp; UBERON=UBERON_0001754.
Disease	Williams syndrome (NCIt: C85232) Williams syndrome (ORDO: Orphanet_904)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_RI98 ! WS77-c1 CVCL_RI99 ! WS77-c4
Sex of cell	Female
Age at sampling	8Y1M
Category	Induced pluripotent stem cell
Publications	PubMed=27509850; DOI=10.1038/nature19067; PMCID=PMC4995142 Chailangkarn T., Trujillo C.A., Freitas B.C., Hrvoj-Mihic B., Herai R.H., Yu D.X., Brown T.T., Marchetto M.C.N., Bardy C., McHenry L., Stefanacci L., Jarvinen A.M., Searcy Y.M., DeWitt M., Wong W., Lai P., Ard M.C., Hanson K.L., Romero S., Jacobs B., Dale A.M., Dai L., Korenberg J.R., Gage F.H., Bellugi U., Halgren E., Semendeferi K., Muotri A.R. A human neurodevelopmental model for Williams syndrome. Nature 536:338-343(2016)
Cell line databases/resources	SKIP; SKIP001244
Encyclopedic resources	Wikidata; Q54994437
Entry history
Entry creation	05-Mar-2018
Last entry update	10-Apr-2025
Version number	7