IFT25
Intraflagellar transport protein 25 homolog
Also known as: C1orf41, FAP232, HSPB11, HSPCO34, IFT25_HUMAN, PP25
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y547
- Gene
- IFT25
- Ensembl
- ENSG00000081870
- Chromosome
- 1
- Canonical length
- 144 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mid piece,Principal piece,End piece
OverviewNCBI Gene
Predicted to enable metal ion binding activity. Predicted to be involved in kidney development; smoothened signaling pathway; and spermatogenesis. Predicted to act upstream of or within several processes, including left/right axis specification; lung development; and skeletal system development. Part of intraciliary transport particle B. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
144 residues, UniProt reviewed canonical sequence.
>Q9Y547|IFT25
1 MRKIDLCLSS EGSEVILATS SDEKHPPENI IDGNPETFWT TTGMFPQEFI ICFHKHVRIE
61 RLVIQSYFVQ TLKIEKSTSK EPVDFEQWIE KDLVHTEGQL QNEEIVAHDG SATYLRFIIV
121 SAFDHFASVH SVSAEGTVVS NLSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against IFT25 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 91 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 91 nTPM
- choroid plexus: 84 nTPM
- fallopian tube: 75 nTPM
- epididymis: 67 nTPM
- lymph node: 58 nTPM
- tonsil: 58 nTPM
Single-cell type
- respiratory ciliated cells: 368 nCPM
- fallopian tube ciliated cells: 319 nCPM
- endometrial ciliated cells: 284 nCPM
- cytotrophoblasts: 219 nCPM
- oocytes: 207 nCPM
- migrating cytotrophoblasts: 189 nCPM
Immune cell
- basophil: 171 nTPM
- eosinophil: 131 nTPM
- T-reg: 122 nTPM
- plasmacytoid DC: 122 nTPM
- NK-cell: 110 nTPM
- memory CD8 T-cell: 105 nTPM
Brain region
- choroid plexus: 48 nTPM
- white matter: 32 nTPM
- cerebral cortex: 31 nTPM
- hypothalamus: 28 nTPM
- spinal cord: 27 nTPM
- basal ganglia: 27 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.35
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- cilium assembly
- heart development
- intraciliary anterograde transport
- kidney development
- left/right axis specification
- lung development
- protein transport
- skeletal system development
- smoothened signaling pathway
- spermatogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Coagulation factor 5/8, C-terminal domain
- Galactose-binding-like domain superfamily
- F5/8 type C domain
- Intraflagellar transport protein 25
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of IFT25 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads IFT25 as an antibody target. Whether an autoantibody or antibody against IFT25 could matter depends on whether native IFT25 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
IFT25 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label IFT25 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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