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Cellosaurus DD2123 (CVCL_9I91)

[Text version]
Cell line name DD2123
Accession CVCL_9I91
Resource Identification Initiative To cite this cell line use: DD2123 (RRID:CVCL_9I91)
Comments Part of: ECACC chromosomal abnormality collection.
Karyotypic information: 47,XY,+13 (ECACC=94110706).
Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Disease Polysyndactyly (NCIt: C125597)
Trisomy 13 (NCIt: C36529)
Polysyndactyly (ORDO: Orphanet_93338)
Trisomy 13 (ORDO: Orphanet_3378)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Fetus
Category Finite cell line
Cross-references
Cell line collections (Providers) ECACC; 94110706
Encyclopedic resources Wikidata; Q54830124
Entry history
Entry creation23-Feb-2016
Last entry update29-Jun-2023
Version number6