Ift122 Gene Summary [Rat]

Predicted to be involved in several processes, including cilium organization; embryonic morphogenesis; and protein localization to organelle. Predicted to act upstream of or within several processes, including embryonic morphogenesis; negative regulation of keratinocyte proliferation; and smoothened signaling pathway involved in dorsal/ventral neural tube patterning. Predicted to be located in several cellular components, including ciliary base; nucleus; and photoreceptor connecting cilium. Predicted to be part of intraciliary transport particle A. Predicted to be active in non-motile cilium. Human ortholog(s) of this gene implicated in cranioectodermal dysplasia 1. Orthologous to human IFT122 (intraflagellar transport 122). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Ift122
Official Name
intraflagellar transport 122 [Source:RGD Symbol;Acc:1311302]
Ensembl ID
ENSRNOG00000010952
Bio databases IDs NCBI: 312651 Ensembl: ENSRNOG00000010952
Aliases intraflagellar transport 122
Synonyms CED, CED1, CFAP80, FAP80, intraflagellar transport 122, sopb, SPG, WDR10, WDR10p, WDR140
Species
Rat, Rattus norvegicus
OrthologiesHumanMouse

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 rat Ift122 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • WD40 repeats
  • WD domain, G-beta repeat
  • WD40
  • protein binding

Pathways

Biological processes and signaling networks where the Ift122 gene in rat plays a role, providing insight into its function and relevance in health or disease.

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • cranioectodermal dysplasia type 1
  • exencephaly
  • polysyndactyly
  • asthma
regulated by
regulates
role in cell
  • proliferation
  • assembly
  • number
  • lack
  • signal transduction in
  • abnormal morphology
  • morphology

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
  • ciliary tip
  • Cytoplasm
  • cilia
  • basal bodies
  • cytosol
  • connecting cilia
  • nucleoplasm
  • nuclear envelope

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the rat Ift122 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • embryonic heart tube left/right pattern formation
  • cilium morphogenesis
  • limb development
  • embryonic body morphogenesis
  • spinal cord dorsal/ventral patterning
  • embryonic heart tube development
  • negative regulation of smoothened signaling pathway
  • establishment of protein localization to organelle
  • camera-type eye morphogenesis
  • intraflagellar transport
  • neural tube closure
  • embryonic forelimb morphogenesis
  • intraflagellar anterograde transport
  • intraflagellar retrograde transport
  • intracellular signal transduction

Cellular Component

Where in the cell the gene product is active
  • photoreceptor connecting cilium
  • cytoplasm
  • cilium basal body
  • membrane
  • cilium
  • intraflagellar transport particle A

Molecular Function

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

Gene-Specific Assays for Results You Can Trust

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