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Cellosaurus GIS2014-SB3C16 (CVCL_QX35)

[Text version]
Cell line name GIS2014-SB3C16
Accession CVCL_QX35
Resource Identification Initiative To cite this cell line use: GIS2014-SB3C16 (RRID:CVCL_QX35)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
Disease Spinal and bulbar muscular atrophy, X-linked 1 (NCIt: C85233)
Kennedy disease (ORDO: Orphanet_481)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 58Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=28395737

Markers:
AmelogeninX,Y
CSF1PO10,12
D1S165610,15
D2S44111,14
D2S133820
D3S135815,16
D5S81812
D7S8208,11
D8S117911,14
D10S124813,15
D12S39115,17
D13S3178
D16S53911
D18S5113
D19S43315,15.2
D21S1128,30
D22S104517,19
DYS39110
FGA23,25
SE3328.2,31.2
TH016,9.3
TPOX8,11
vWA14,17

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Publications

PubMed=28395737; DOI=10.1016/j.scr.2017.02.005
Narayanan G., Sheila M., Chai J., Stanton L.W.
Generation of sibling-matched induced pluripotent stem cell lines from spinal and bulbar muscular atrophy patients.
Stem Cell Res. 20:30-33(2017)

Cross-references
Encyclopedic resources Wikidata; Q54835839
Entry history
Entry creation15-Nov-2017
Last entry update19-Dec-2024
Version number9