ATP6V1G2-DDX39B Gene Summary [Human]

This locus represents naturally occurring read-through transcription between the neighboring ATP6V1G2 (ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2) and DDX39B (DEAD box polypeptide 39B) genes located in the major histocompatibility complex class III region of chromosome 6. The read-through transcript and is a candidate for nonsense-mediated mRNA decay (NMD), and is thus unlikely to produce a protein product. [provided by RefSeq, Feb 2011]

Details

Type
Nonsense Mediated Decay
Official Symbol
ATP6V1G2-DDX39B
Official Name
ATP6V1G2-DDX39B readthrough (NMD candidate) [Source:HGNC Symbol;Acc:HGNC:41999]
Ensembl ID
ENSG00000254870
Bio databases IDs NCBI: 100532737 Ensembl: ENSG00000254870
Aliases ATP6V1G2-DDX39B readthrough (NMD candidate)
Synonyms ATP6V1G2-DDX39B readthrough (NMD candidate), BX248516.1
Species
Human, Homo sapiens

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
regulated by
disease
  • atopic dermatitis
  • Stevens-Johnson syndrome
  • toxic epidermal necrolysis

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Unknown

Gene-Specific Assays for Results You Can Trust

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