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Cellosaurus VUB13_FXS (CVCL_9849)

[Text version]

Cell line name VUB13_FXS
Synonyms VUBe012-A
Accession CVCL_9849
Resource Identification Initiative To cite this cell line use: VUB13_FXS (RRID:CVCL_9849)
Comments From: Vrije Universiteit Brussel; Brussels; Belgium.
Sequence variations Mutation; HGNC; 3775; FMR1; Repeat_expansion; CGG[2000]; 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
Web pages http://emgerege.vub.ac.be/HESC_2.php
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
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; VUBe012-A
ISCR; 240
SKIP; SKIP001835
Other Wikidata; Q54993398
Entry history
Entry creation06-Jun-2012
Last entry update20-May-2021
Version number14