Transcriptome analysis of CDAN1 deficiency in human erythroleukemic K562 cells.
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ABSTRACT: Congenital dyserythropoietic anemia Type 1 (CDA1) is a rare macrocytic anemia caused by loss-of-function mutation of CDAN1. To investigate the functional role of CDAN1, we performed RNA-sequencing on human erythroleukemic K562 cells with CDAN1 shRNA knockdown using a doxycycline inducible system
ORGANISM(S): Homo sapiens
PROVIDER: GSE225925 | GEO | 2024/06/30
REPOSITORIES: GEO
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