FAM219A Gene Summary [Human]

The protein encoded by this gene has homologs that have been identified in mouse, macaque, etc organisms. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Dec 2010]

Details

Type
Protein Coding
Official Symbol
FAM219A
Official Name
family with sequence similarity 219 member A [Source:HGNC Symbol;Acc:HGNC:19920]
Ensembl ID
ENSG00000164970
Bio databases IDs NCBI: 203259 Ensembl: ENSG00000164970
Aliases family with sequence similarity 219 member A
Synonyms 2310028H24Rik, C9orf25, family with sequence similarity 219 member A, family with sequence similarity 219, member A, LOC684046
Species
Human, Homo sapiens
OrthologiesMouseRat

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 FAM219A often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Protein family FAM219A
  • protein binding

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • metabolic syndrome X
  • diabetic nephropathy
regulated by

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.