NME1-NME2 Gene Summary [Human]

This locus represents naturally occurring read-through transcription between the neighboring NME1 and NME2 genes. The significance of this read-through transcription and the function of the resulting protein product have not yet been determined. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2010]

Details

Type
Protein Coding
Official Symbol
NME1-NME2
Official Name
NME1-NME2 readthrough [Source:HGNC Symbol;Acc:HGNC:33531]
Ensembl ID
ENSG00000011052
Bio databases IDs NCBI: 654364 Ensembl: ENSG00000011052
Aliases NME1-NME2 readthrough
Synonyms NM23-LV, NME1-NME2 readthrough, NMELV
Species
Human, Homo sapiens

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human NME1-NME2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • nucleoside diphosphate kinase
  • Nucleoside diphosphate kinase family
  • NDPk

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.

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

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.