FAM234A Gene Summary [Human]

Located in cell surface. [provided by Alliance of Genome Resources, Apr 2022]

Details

Type
Nonsense Mediated Decay
Official Symbol
FAM234A
Official Name
family with sequence similarity 234 member A [Source:HGNC Symbol;Acc:HGNC:14163]
Ensembl ID
ENSG00000167930
Bio databases IDs NCBI: 83986 Ensembl: ENSG00000167930
Aliases family with sequence similarity 234 member A
Synonyms C16ORF9, DKFZP761D0211, family with sequence similarity 234 member A, family with sequence similarity 234, member A, gs19, ITFG3, LOC100365269, RGD1311484
Species
Human, Homo sapiens
OrthologiesMouse

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • non-insulin-dependent diabetes mellitus
  • diabetes mellitus
  • migraines
  • iron deficiency anemia
  • familial hemolytic anemia
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.
  • Plasma Membrane
  • cell surface

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human FAM234A gene, providing context for its role in the cell.

Cellular Component

Where in the cell the gene product is active
  • extracellular vesicular exosome
  • membrane
  • cell surface

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.