Cellosaurus cell line 110150C (CVCL

Cross-references
Cell line name	110150C
Accession	CVCL_VG26
Resource Identification Initiative	To cite this cell line use: 110150C (RRID:CVCL_VG26)
Comments	Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:5173; HRAS; Simple; p.Gly12Ser (c.34G>A); ClinVar=VCV000012602; Zygosity=Unspecified (PubMed=26740656).
Disease	Costello syndrome (NCIt: C84652) Costello syndrome (ORDO: Orphanet_3071)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Female
Age at sampling	1Y
Category	Induced pluripotent stem cell
Publications	PubMed=26740656; DOI=10.1523/JNEUROSCI.1547-15.2016; PMCID=PMC4701956 Rooney G.E., Goodwin A.F., Depeille P., Sharir A., Schofield C.M., Yeh E., Roose J.P., Klein O.D., Rauen K.A., Weiss L.A., Ullian E.M. Human iPS cell-derived neurons uncover the impact of increased Ras signaling in Costello syndrome. J. Neurosci. 36:142-152(2016)
Cell line databases/resources	SKIP; SKIP001326
Encyclopedic resources	Wikidata; Q54399987
Entry history
Entry creation	14-May-2018
Last entry update	19-Dec-2024
Version number	10