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Cellosaurus ERPLi002-A (CVCL_YT21)

[Text version]
Cell line name ERPLi002-A
Synonyms PD24072008
Accession CVCL_YT21
Resource Identification Initiative To cite this cell line use: ERPLi002-A (RRID:CVCL_YT21)
Comments From: Eyestem Research Private Ltd; Bangalore; India.
Population: Indian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
Disease Leber congenital amaurosis (NCIt: C129075)
Leber congenital amaurosis (ORDO: Orphanet_65)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 11Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=32278301

Markers:
AmelogeninX,Y
CSF1PO11,12
D2S133817,20
D3S135815
D5S81810,13
D7S82011,13
D8S117911,13
D13S3178,11
D16S53910,14
D18S5115
D19S43313,14.2
D21S1131.2,33.2
FGA20,22
TH016,7
TPOX8,11
vWA15,16

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Publications

PubMed=32278301; DOI=10.1016/j.scr.2020.101757
Konala V.B.R., Nandakumar S., Battu R., Pal R.
Derivation of three induced pluripotent stem cell lines under feeder-free culture conditions from peripheral blood mononuclear cells (PBMC) of Indian patients suffering from inherited retinal diseases carrying different mutations.
Stem Cell Res. 45:101757-101757(2020)

Cross-references
Cell line databases/resources hPSCreg; ERPLi002-A
SKIP; SKIP005736
Encyclopedic resources Wikidata; Q93541815
Entry history
Entry creation12-Mar-2020
Last entry update19-Dec-2024
Version number8