Ift52 Gene Summary [Mouse]

Acts upstream of or within several processes, including embryonic morphogenesis; negative regulation of keratinocyte proliferation; and non-motile cilium assembly. Located in several cellular components, including ciliary base; ciliary tip; and microtubule organizing center. Part of intraciliary transport particle B. Human ortholog(s) of this gene implicated in asphyxiating thoracic dystrophy. Orthologous to human IFT52 (intraflagellar transport 52). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Ift52
Official Name
intraflagellar transport 52 [Source:MGI Symbol;Acc:MGI:2387217]
Ensembl ID
ENSMUSG00000017858
Bio databases IDs NCBI: 245866 Ensembl: ENSMUSG00000017858
Aliases intraflagellar transport 52
Synonyms AU015812, C20orf9, CGI-53, intraflagellar transport 52, LOC684302, NGD2, NGD5, RGD1311004
Species
Mouse, Mus musculus
OrthologiesHumanRat

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 mouse Ift52 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 binding

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • short-rib thoracic dysplasia type 16 with polydactyly
  • non-insulin-dependent diabetes mellitus
  • short rib-polydactyly syndrome
  • short-rib thoracic dysplasia type 16 with or without polydactyly
  • short-rib thoracic dysplasia 16 without polydactyly
role in cell
  • proliferation
  • assembly
  • clustering in
  • clustering

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Extracellular Space
  • motile cilia
  • ciliary tip
  • non-motile cilium
  • cilia
  • basal bodies
  • centrosome
  • centriole
  • connecting cilia
  • neurites
  • dendrites

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Ift52 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • negative regulation of keratinocyte proliferation
  • neural tube formation
  • keratinocyte proliferation
  • cilium morphogenesis
  • intraflagellar transport
  • smoothened signaling pathway
  • heart looping
  • intraflagellar anterograde transport
  • dorsal/ventral pattern formation
  • embryonic digit morphogenesis
  • regulation of protein processing

Cellular Component

Where in the cell the gene product is active
  • dendrite terminus
  • photoreceptor connecting cilium
  • motile cilium
  • centrosome
  • cilium basal body
  • centriole
  • cilium
  • intraflagellar transport particle B

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.