FXYD6-FXYD2 Gene Summary [Human]

This locus represents naturally occurring read-through transcription between the neighboring FXYD domain-containing ion transport regulator 6 (GeneID 53826) and sodium/potassium-transporting ATPase subunit gamma (GeneID 486) genes on chromosome 11. One read-through transcript produces a fusion protein that shares sequence identity with each individual gene product, while another read-through transcript encodes a protein that has a distinct C-terminus and only shares sequence identity with the upstream locus (GeneID 53826). [provided by RefSeq, Aug 2011]

Details

Type
Protein Coding
Official Symbol
FXYD6-FXYD2
Official Name
FXYD6-FXYD2 readthrough [Source:HGNC Symbol;Acc:HGNC:39978]
Ensembl ID
ENSG00000255245
Bio databases IDs NCBI: 100533181 Ensembl: ENSG00000255245
Aliases FXYD6-FXYD2 readthrough
Synonyms FXYD6, FXYD6-FXYD2 readthrough
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 FXYD6-FXYD2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • ATP1G1/PLM/MAT8 family
  • phenylalanine-X-tyrosine-aspartate (FXYD) family

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • renal hypomagnesemia type 2

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.