FAM161A Gene Summary [Human]

This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011]

Details

Type
Nonsense Mediated Decay
Official Symbol
FAM161A
Official Name
FAM161 centrosomal protein A [Source:HGNC Symbol;Acc:HGNC:25808]
Ensembl ID
ENSG00000170264
Bio databases IDs NCBI: 84140 Ensembl: ENSG00000170264
Aliases FAM161 centrosomal protein A
Synonyms 4930430E16Rik, FAM161 centrosomal protein A, family with sequence similarity 161, member A, RGD1304999, RP28
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 FAM161A often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • microtubule binding
  • Uncharacterized protein family UPF0564
  • protein binding
  • identical 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
  • hereditary disorder
  • retinitis pigmentosa type 28
  • retinal dystrophy
  • retinitis pigmentosa
  • cone-rod dystrophy
  • autosomal recessive retinitis pigmentosa
  • early-onset high myopia
regulated by
role in cell
  • assembly
  • organization

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • non-motile cilium
  • basal bodies
  • centrosome
  • Golgi Apparatus
  • centriole
  • cytosol
  • connecting cilia
  • nucleoplasm
  • spindle pole
  • spindle fibers
  • neurites
  • photoreceptor inner segments
  • astral microtubules
  • mitotic spindle

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human FAM161A gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • cilium morphogenesis
  • visual perception

Cellular Component

Where in the cell the gene product is active
  • photoreceptor connecting cilium
  • spindle microtubule
  • centrosome
  • mitotic spindle
  • cilium basal body
  • cilium
  • photoreceptor inner segment
  • astral microtubule

Molecular Function

What the gene product does at the molecular level
  • identical protein binding
  • protein binding
  • microtubule 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.