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Long intergenic non-protein coding RNA 1965 (LINC01965)

Target
LINC01965
Molecular classification
Long intergenic non-coding RNA (lincRNA), Long non-coding RNA (lncRNA), Non-coding RNA
01

Overview

Long intergenic non-protein coding RNA 1965 (LINC01965) is a human non-coding RNA gene, classified as a long intergenic non-coding RNA (lincRNA), meaning it is an autonomously transcribed, spliced RNA transcript longer than 200 nucleotides that does not overlap coding genes[1][5][3]. LincRNAs, including LINC01965, are thought to regulate gene expression at multiple levels, potentially affecting chromatin state, nuclear structure, or local transcriptional environments, often with high tissue and disease specificity[3][9]. There are currently no specific biological functions, disease mechanisms, or drug interactions directly attributed to LINC01965, although it has surfaced as a locus in large-scale genetic studies of neurological and psychiatric traits[2][4][6]. The functional and therapeutic relevance of LINC01965 remains to be established.

02

Mechanism of action

No therapeutic mechanism of action is reported for the direct targeting of LINC01965. Functional modulation, if it becomes of interest, would likely involve RNA interference, antisense oligonucleotides, or genome-editing approaches, but no clinical data support this at present[3][6][8].

03

Biological functions

Regulation of gene expression (via chromatin remodeling, transcriptional or post-transcriptional regulation, enhancer-associated activity)Genome architecture modulation (indirect evidence from lincRNA properties)Tissue-specific expression (common to lincRNAs, role in specific brain regions inferred by context; direct functional assignment for LINC01965 is currently unavailable)
04

Disease associations

Genetic association studies have implicated loci near LINC01965 in epilepsy, particularly genetic generalized epilepsy and related morphometric brain endophenotypesGenetic risk for suicidal behavior: LINC01965 is mentioned among loci identified in at least one genome-wide association study in the context of suicide attempt riskCancer (glioma): Some large-scale brain-specific eQTL and pharmacogenomic screens included LINC01965, though no causal or mechanistic role has been assigned

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