Cellosaurus cell line WC005i-FX11-7 (CVCL

Cross-references
Cell line name	WC005i-FX11-7
Synonyms	FX11-7
Accession	CVCL_EJ76
Resource Identification Initiative	To cite this cell line use: WC005i-FX11-7 (RRID:CVCL_EJ76)
Comments	Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; 3775; FMR1; Repeat_expansion; CGG[>435]; ClinVar=VCV000009972; Zygosity=Hemizygous (PubMed=24654675).
Disease	Fragile X syndrome (NCIt: C84717) Fragile X syndrome (ORDO: Orphanet_908)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_EJ77 ! WC006i-FX11-9U
Sex of cell	Male
Age at sampling	7Y
Category	Induced pluripotent stem cell
Publications	PubMed=24654675; DOI=10.1089/scd.2014.0030; PMCID=PMC4103262 Doers M.E., Musser M.T., Nichol R., Berndt E.R., Baker M., Gomez T.M., Zhang S.-C., Abbeduto L., Bhattacharyya A. iPSC-derived forebrain neurons from FXS individuals show defects in initial neurite outgrowth. Stem Cells Dev. 23:1777-1787(2014)
Cell line collections (Providers)	WiCell; wc005i-fx11-7
Encyclopedic resources	Wikidata; Q54993616
Entry history
Entry creation	26-Sep-2016
Last entry update	29-Jun-2023
Version number	12