Solute carrier family 23 member 3–Non-homologous end joining factor 1 readthrough (SLC23A3-NHEJ1 readthrough)

The "SLC23A3-NHEJ1 readthrough" (ENSG00000280537) refers to a predicted fusion transcript generated by transcriptional readthrough between the SLC23A3 and NHEJ1 genes. While both parent genes encode proteins with distinct cellular functions—SLC23A3 encodes a transmembrane transporter for hypoxanthine, and NHEJ1 encodes a DNA repair factor—there is no evidence that the readthrough transcript encodes a functional protein or that it has specific biological, disease, or pharmacological relevance. This entity is likely the result of annotation or prediction pipelines identifying rare transcriptional or splicing events, rather than a validated molecular target. No direct aliases, classifications, functions, associated diseases, drugs, biomarkers, or safety concerns exist for this readthrough product; any relevant information applies only to the separate parental genes[2][5][4].

Other names

SLC23A3-NHEJ1 readthroughSolute carrier family 23 member 3–non-homologous end joining factor 1 fusionENSG00000280537 (Ensembl gene ID)

None known.