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ProteomicsHYDIN2 knockdown in NT2 cells analyses by LFQ
Segmental duplications at proximal loci can generate transcriptionally active chimeric pseudogenes (φgenes) by fusing contiguous sequences from two parental genes. These chimeric φgenes often co-opt 5′ regulatory elements for activation and acquire 3′ modifications that enhance transcript stability,...
ORGANISM(S): Homo sapiens (Human) 
2026-05-25 | PXD074698 | Pride
Hydin2 Chimeric pseudogene Lfq proteomics 
GenomicsAnalysis of transcriptomic alterations in HYDIN2 knockdown as compared to empty vector control in NT2 cells
Analysis of transcriptomic alterations in HYDIN2 knockdown as compared to empty vector control in NT2 cells
PRJNA1268351 | ENA
TranscriptomicsAnalysis of transcriptomic alterations in HYDIN2 knockdown as compared to empty vector control in NT2 cells
Transcriptomic analysis was performed to identify differentially expressed genes under HYDIN2 knockdown conditions compared to an empty vector control. Pathway enrichment analysis revealed a significant upregulation of neuronal-related pathways and a downregulation of those involved in fundamental c...
ORGANISM(S): Homo sapiens 
2025-10-07 | GSE298099 | GEO
GenomicsHomo sapiens
Targeted long-read RNA sequencing of human HYDIN2
PRJNA359986 | ENA
UnknownThe birth of a human-specific neural gene by incomplete duplication and gene fusion.
Not available
S-EPMC5345166 | biostudies-literature
UnknownCombined approaches, including long-read sequencing, address the diagnostic challenge of HYDIN in primary ciliary dyskinesia.
Not available
S-EPMC11369241 | biostudies-literature
UnknownLong-Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia.
Not available
S-EPMC12674883 | biostudies-literature
UnknownInfluence of <i>cis</i>-regulatory elements on expression divergence in human segmental duplications.
Not available
S-EPMC12642434 | biostudies-literature
UnknownRecessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry.
Not available
S-EPMC3484652 | biostudies-literature
UnknownPathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility.
Not available
S-EPMC9981940 | biostudies-literature
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