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Cellosaurus GIS2014-SB2C20 (CVCL_QX34)

[Text version]
Cell line name GIS2014-SB2C20
Accession CVCL_QX34
Resource Identification Initiative To cite this cell line use: GIS2014-SB2C20 (RRID:CVCL_QX34)
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 55Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=28395737

Markers:
AmelogeninX,Y
CSF1PO11
D1S165616,17.3
D2S44110,12
D2S133818
D3S135815,16
D5S81811
D7S8208,13
D8S117914,15
D10S124813,14
D12S39119,21
D13S3178,10
D16S5399,11
D18S5115,16
D19S43313
D21S1129,30
D22S104515,17
DYS3916
FGA20,22
SE3315,30.2
TH019,9.3
TPOX8
vWA14,17

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Publications

PubMed=28395737; DOI=10.1016/j.scr.2017.02.005
Gunaseelan Narayanan, Marianne Sheila, Josiah Chai, Lawrence Walter Stanton;
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; Q54835838
Entry history
Entry creation15-Nov-2017
Last entry update19-Dec-2024
Version number9