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Cellosaurus GENEA078 (CVCL_B886)

[Text version]
Cell line name GENEA078
Synonyms Genea078; SIVF078
Accession CVCL_B886
Resource Identification Initiative To cite this cell line use: GENEA078 (RRID:CVCL_B886)
Comments From: Genea Biocells, Ltd; Sydney; Australia.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-14-0252.
Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-50.
Donor information: Embryo is sibling to those giving rise to GENEA079 (Cellosaurus=CVCL_B887) and GENEA080 (Cellosaurus=CVCL_B888).
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Sequence variations
  • Mutation; HGNC; HGNC:7720; NEB; Simple; c.15110dupA; Zygosity=Heterozygous (PubMed=27346006).
  • Mutation; HGNC; HGNC:7720; NEB; Unexplicit; Ex55del; Zygosity=Heterozygous (PubMed=27346006).
Disease Nemaline myopathy 2 (NCIt: C118784)
Typical nemaline myopathy (ORDO: Orphanet_171436)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Blastocyst stage
Category Embryonic stem cell
STR profile Source(s): PubMed=27346006

Markers:
AmelogeninX
CSF1PO10,11
D2S133817,24
D3S135815
D5S81812,13
D7S8208,10
D8S117911,13
D13S31711
D16S53912
D18S5112,13
D19S43314,15
D21S1128,30
FGA22,23
TH016
TPOX8
vWA16,17

Run an STR similarity search on this cell line
Web pages https://web.archive.org/web/20180912205435/http://geneabiocells.com/services/shelf-products/human-embryonic-stem-cells/
Publications

PubMed=27346006; DOI=10.1016/j.scr.2016.02.004
Dumevska B., Main H., McKernan R., Goel D., Schmidt U.
Derivation of NEM2 affected human embryonic stem cell line Genea078.
Stem Cell Res. 16:427-429(2016)

Cross-references
Cell line databases/resources NIHhESC; NIHhESC-14-0252
Encyclopedic resources Wikidata; Q54835649
Entry history
Entry creation06-Jun-2012
Last entry update19-Dec-2024
Version number20