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Cellosaurus SZ-FX14 (CVCL_YL37)

[Text version]
Cell line name SZ-FX14
Synonyms SZ-FX14 PGD; FX#14
Accession CVCL_YL37
Resource Identification Initiative To cite this cell line use: SZ-FX14 (RRID:CVCL_YL37)
Comments From: Shaare Zedek Medical Center, The Hebrew University; Jerusalem; Israel.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-20-0450.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Sequence variations
Disease Fragile X syndrome (NCIt: C84717)
Fragile X syndrome (ORDO: Orphanet_908)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Blastocyst stage
Category Embryonic stem cell
Web pages https://www.szmc.org.il/UploadFiles/12_2016/HESC.pdf
Publications

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 NIHhESC; NIHhESC-20-0450
Encyclopedic resources Wikidata; Q98133002
Entry history
Entry creation19-Dec-2019
Last entry update19-Dec-2024
Version number8