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Cellosaurus TVGH-iPSC-010-09 (CVCL_RP84)

[Text version]
Cell line name TVGH-iPSC-010-09
Synonyms TVGHi001-A
Accession CVCL_RP84
Resource Identification Initiative To cite this cell line use: TVGH-iPSC-010-09 (RRID:CVCL_RP84)
Comments From: Taipei Veterans General Hospital; Taipei; Taiwan.
Population: Chinese; Taiwan.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
Disease Leber hereditary optic atrophy (NCIt: C84808)
Leber hereditary optic neuropathy (ORDO: Orphanet_104)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 61Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=29427840

Markers:
AmelogeninX
CSF1PO11,12
D2S133819,25
D3S135815,16
D5S81810,12
D7S82011,12
D8S117911,16
D13S31711,12
D16S53910,11
D18S5111,14
D19S43314,14.2
D21S1128,30.2
FGA23,25
TH017,10
TPOX8,11
vWA17,19

Run an STR similarity search on this cell line
Publications

PubMed=29427840; DOI=10.1016/j.scr.2018.01.029
Lu H.-E., Yang Y.-P., Chen Y.-T., Wu Y.-R., Wang C.-L., Tsai F.-T., Hwang D.-K., Lin T.-C., Chen S.-J., Wang A.-G., Hsieh P.C.-H., Chiou S.-H.
Generation of patient-specific induced pluripotent stem cells from Leber's hereditary optic neuropathy.
Stem Cell Res. 28:56-60(2018)

Cross-references
Cell line collections (Providers) BCRC; SC81071
Cell line databases/resources hPSCreg; TVGHi001-A - Discontinued
SKIP; SKIP003129
SKIP; SKIP005667
Encyclopedic resources Wikidata; Q54973395
Entry history
Entry creation05-Mar-2018
Last entry update19-Dec-2024
Version number11