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Cellosaurus CRTDi006-B (CVCL_C1YD)

[Text version]
Cell line name CRTDi006-B
Synonyms AGS1V201D_2
Accession CVCL_C1YD
Resource Identification Initiative To cite this cell line use: CRTDi006-B (RRID:CVCL_C1YD)
Comments From: Center for Regenerative Therapies Dresden (CRTD); Dresden; Germany.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Aicardi-Goutieres syndrome 1 (NCIt: C165501)
Aicardi-Goutieres syndrome (ORDO: Orphanet_51)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C1P2 ! CRTDi006-A
Sex of cell Male
Age at sampling 11Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=36027857

Markers:
AmelogeninX,Y
CSF1PO11
D2S133819,25
D3S135818
D5S81812
D7S8208,10
D8S117910,12
D13S3178,11
D16S53914
D18S5113
D19S43316.2
D21S1130
FGA21,23
TH016,9.3
TPOX8,12
vWA18,19

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Publications

PubMed=36027857; DOI=10.1016/j.scr.2022.102895
Hanchen V., Kretschmer S., Wolf C., Engel K., Khattak S., Neumann K., Lee-Kirsch M.A.
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutieres syndrome type 1 due to biallelic TREX1 mutations.
Stem Cell Res. 64:102895-102895(2022)

Cross-references
Cell line databases/resources hPSCreg; CRTDi006-B
Biological sample resources BioSamples; SAMEA13151271
Encyclopedic resources Wikidata; Q114311270
Entry history
Entry creation22-Sep-2022
Last entry update19-Dec-2024
Version number5