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Cellosaurus VUB11_FXS (CVCL_9848)

[Text version]
Cell line name VUB11_FXS
Synonyms VUBe011-A
Accession CVCL_9848
Resource Identification Initiative To cite this cell line use: VUB11_FXS (RRID:CVCL_9848)
Comments From: Vrije Universiteit Brussel; Brussels; Belgium.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Sequence variations
  • Mutation; HGNC; 3775; FMR1; Repeat_expansion; CGG[2000-2010]; ClinVar=VCV000009972; Zygosity=Unspecified (PubMed=27690107).
Disease Fragile X syndrome (NCIt: C84717)
Fragile X syndrome (ORDO: Orphanet_908)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Blastocyst stage
Category Embryonic stem cell
Publications

PubMed=20224973; DOI=10.1007/s11626-010-9284-4
Mateizel I., Spits C., De Rycke M., Liebaers I., Sermon K.
Derivation, culture, and characterization of VUB hESC lines.
In Vitro Cell. Dev. Biol. Anim. 46:300-308(2010)

PubMed=27690107; DOI=10.3390/genes7100077; PMCID=PMC5083916
Mor-Shaked H., Eiges R.
Modeling fragile X syndrome using human pluripotent stem cells.
Genes (Basel) 7:77.1-77.19(2016)

Cross-references
Cell line databases/resources hPSCreg; VUBe011-A
SKIP; SKIP001834
Encyclopedic resources Wikidata; Q54993397
Entry history
Entry creation06-Jun-2012
Last entry update10-Sep-2024
Version number18