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Cellosaurus WAe009-A-82 (CVCL_B5QN)

[Text version]
Cell line name WAe009-A-82
Synonyms SMUDHe010-A-82
Accession CVCL_B5QN
Resource Identification Initiative To cite this cell line use: WAe009-A-82 (RRID:CVCL_B5QN)
Comments From: Southern Medical University; Guangzhou; China.
Sequence variations
  • Mutation; HGNC; 8507; OSMR; Simple_edited; p.Gly513Asp (c.1538G>A); ClinVar=VCV000802119; Zygosity=Homozygous; Note=By CRISPR/Cas9 (PubMed=35714449).
Disease Familial primary localized cutaneous amyloidosis-1 (NCIt: C189282)
Familial primary localized cutaneous amyloidosis (ORDO: Orphanet_353220)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_9773 (WA09)
Sex of cell Female
Age at sampling Blastocyst stage
Category Embryonic stem cell

PubMed=35714449; DOI=10.1016/j.scr.2022.102842
Zheng W., Zhong Y.-D., Yuan L.-Y., Yu X.-L., Wang X., Yang C., Liu H.-T., Lv P., Luo Y.-Y., Qiu B.-Y., Liu J., Yang B.
Generation of a human embryonic stem cell line (SMUDHe010-A-82) carrying a homozygous c.1538G > A (p.G513D) mutation in the OSMR gene by CRISPR/Cas9-mediated homologous recombination.
Stem Cell Res. 63:102842-102842(2022)

Cell line databases/resources hPSCreg; WAe009-A-82
Biological sample resources BioSamples; SAMEA12121387
Encyclopedic resources Wikidata; Q112041926
Entry history
Entry creation17-Mar-2022
Last entry update21-Mar-2023
Version number4