CVCL_9I99 - Rat Genome Database

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Cell Line : CVCL_9I99 (DD2135) Homo sapiens

Symbol: CVCL_9I99
Name: DD2135
RGD ID: 21135006
Cell Line Type: finite cell line
Origin: Karyotypic information: 47,XYY (ECACC=94112416); Derived from site: In situ; Fetal muscle; UBERON=UBERON_0001630; Cell type: Fibroblast of muscle; CL=CL_1001609.
Gender: Male
Groups: Part of: ECACC chromosomal abnormality collection
Originate from same individual as: CVCL_9I85 (DD2111)
Disease(s): 47, XYY Syndrome (DOID:9001280) [NCI:C85237]

References

Additional Information

Database Acc Id Source(s)
Cellosaurus CVCL_9I99 CELLOSAURUS
ECACC 94112416 CELLOSAURUS
NCIt C85237 CELLOSAURUS
Orphanet 8 CELLOSAURUS
Wikidata Q54830132 CELLOSAURUS