FAM222B Gene Summary [Human]

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

Details

Type
Protein Coding
Official Symbol
FAM222B
Official Name
family with sequence similarity 222 member B [Source:HGNC Symbol;Acc:HGNC:25563]
Ensembl ID
ENSG00000173065
Bio databases IDs NCBI: 55731 Ensembl: ENSG00000173065
Aliases family with sequence similarity 222 member B
Synonyms 9630020I17RIK, C17orf63, family with sequence similarity 222 member B, family with sequence similarity 222, member B, RGD1566149
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 FAM222B 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 of FAM222A
  • 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
  • insomnia
  • non-insulin-dependent diabetes mellitus
  • breast adenocarcinoma
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.
  • Nucleus
  • Mitochondria
  • nucleoplasm

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human FAM222B gene, providing context for its role in the cell.

Cellular Component

Where in the cell the gene product is active
  • nucleoplasm

Molecular Function

What the gene product does at the molecular level
  • protein binding

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.