Chromosome 2 open reading frame 76 (C2orf76)

Chromosome 2 open reading frame 76 (C2orf76) is a protein-coding gene of unknown or poorly characterized function in humans. It is not currently annotated as a therapeutic target such as a receptor, enzyme, transporter, or ion channel[3][1]. C2orf76 is listed in major protein and gene databases, and has associations with a variety of biological entities, tissues, and gene expression datasets, but there is no clear evidence for a specific molecular function, involvement in major signaling or regulatory pathways, or role in known human disease mechanisms[3][1][7]. Current data suggest that, if functional, it may be involved in gene regulatory or epigenetic mechanisms[1]. There are no known drugs, disease biomarkers, or clinical safety issues associated with this gene or its protein product.

Other names

AIM29MGC104437LOC130355UPF0538 protein C2orf76