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novel transcript, antisense to Chromosome 6 open reading frame 89 (ENSG00000298791)

Target
ENSG00000298791
Molecular classification
Other (long non-coding RNA/antisense RNA), Antisense transcript (from gene annotation conventions), Not a protein-coding gene
01

Overview

This entity is an uncharacterized *antisense transcript* located at the C6orf89 locus on chromosome 6 (Ensembl: ENSG00000298791)[7]. It does not code for protein and is annotated as a long non-coding RNA (lncRNA); there are no functional data, publications, or experimental studies describing its biological or disease relevance. Standard databases (Ensembl, NCBI, UniProt) list only its sequence and locus; there is no information supporting its activity, disease association, or role as a drug target. Its canonical related gene, C6orf89, encodes a protein (Chromosome 6 open reading frame 89, also known as bombesin receptor‐activated protein) involved in chromatin remodeling, epithelial proliferation, and wound healing[1][3][11][13][15]. However, this antisense entry (ENSG00000298791) itself is not validated or described as a target, receptor, enzyme, or marker in current biomedical literature or databases. Summary: This is most likely a technical annotation for an uncharacterized, presumably non-coding RNA at the C6orf89 locus. It is not a therapeutic target, is missing biological information, and should not be considered equivalent to the protein or canonical function associated with C6orf89. The entry is primarily useful for gene structure annotation, not for structured biomedical ontology or drug development[7][9][15].

Other names
ENSG00000298791antisense to C6orf89novel antisense transcript at C6orf89 locus
02

Mechanism of action

Not applicable (no drug or experimental data)

03

Biological functions

Unknown (no experimental confirmation; antisense RNAs may regulate parental gene expression, but nothing is demonstrated for this locus)Putative transcriptional regulation of C6orf89
04

Disease associations

None confirmedNo reported association with disease or phenotype

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