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Cellosaurus PHAi001-B (CVCL_YM62)

[Text version]
Cell line name PHAi001-B
Synonyms iPSC-QPH01-II; PIDi001-B
Accession CVCL_YM62
Resource Identification Initiative To cite this cell line use: PHAi001-B (RRID:CVCL_YM62)
Comments From: Pan-Hammarstrom Laboratory, Karolinska Institutet; Stockholm; Sweden.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Immunoglobulin A deficiency 1 (NCIt: C123434)
Recurrent infections associated with rare immunoglobulin isotypes deficiency (ORDO: Orphanet_183675)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_YM61 ! PHAi001-A
Sex of cell Male
Age at sampling 34Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=31689593

Markers:
AmelogeninX,Y
CSF1PO13
D1S165612,17.2
D2S44114,16
D2S133817,21
D3S135816,17
D5S81810,12
D7S8209,10
D8S117910
D10S124815
D12S39117,24
D13S31710,11
D16S53911,12
D18S5114,16
D19S43315,16
D21S1128,31.2
D22S104511,15
DYS39110
FGA20,22
SE3316,20
TH016,9.3
TPOX8,11
vWA18

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Publications

PubMed=31689593; DOI=10.1016/j.scr.2019.101613
Arias-Fuenzalida J., Yu J.-W., Du L.-K., Custodio J., Notarangelo L.D., Hammarstrom L., Pan-Hammarstrom Q.
Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency.
Stem Cell Res. 41:101613-101613(2019)

Cross-references
Cell line databases/resources hPSCreg; PHAi001-B
Encyclopedic resources Wikidata; Q98128580
Entry history
Entry creation12-Mar-2020
Last entry update29-Jun-2023
Version number5