FYTTD1
UAP56-interacting factor
Also known as: DKFZp761B1514, UIF, UIF_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96QD9
- Gene
- FYTTD1
- Ensembl
- ENSG00000122068
- Chromosome
- 3
- Canonical length
- 318 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Nuclear speckles,Cytosol
OverviewNCBI Gene
Enables mRNA binding activity. Involved in mRNA export from nucleus. Located in cytosol; nuclear speck; and nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
318 residues, UniProt reviewed canonical sequence.
>Q96QD9|FYTTD1
1 MNRFGTRLVG ATATSSPPPK ARSNENLDKI DMSLDDIIKL NRKEGKKQNF PRLNRRLLQQ
61 SGAQQFRMRV RWGIQQNSGF GKTSLNRRGR VMPGKRRPNG VITGLAARKT TGIRKGISPM
121 NRPPLSDKNI EQYFPVLKRK ANLLRQNEGQ RKPVAVLKRP SQLSRKNNIP ANFTRSGNKL
181 NHQKDTRQAT FLFRRGLKVQ AQLNTEQLLD DVVAKRTRQW RTSTTNGGIL TVSIDNPGAV
241 QCPVTQKPRL TRTAVPSFLT KREQSDVKKV PKGVPLQFDI NSVGKQTGMT LNERFGILKE
301 QRATLTYNKG GSRFVTVGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FYTTD1 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)
- 0.66
- Highest tissue expression
- 87 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 87 nTPM
- tongue: 63 nTPM
- esophagus: 41 nTPM
- heart muscle: 39 nTPM
- testis: 38 nTPM
- bone marrow: 37 nTPM
Single-cell type
- pdcs: 247 nCPM
- esophageal apical cells: 244 nCPM
- cardiomyocytes: 214 nCPM
- ocular epithelial cells: 160 nCPM
- suprabasal keratinocytes: 111 nCPM
- esophageal suprabasal cells: 107 nCPM
Immune cell
- NK-cell: 65 nTPM
- basophil: 59 nTPM
- total PBMC: 46 nTPM
- MAIT T-cell: 41 nTPM
- memory CD8 T-cell: 36 nTPM
- naive CD4 T-cell: 34 nTPM
Brain region
- cerebellum: 41 nTPM
- hypothalamus: 39 nTPM
- cerebral cortex: 38 nTPM
- white matter: 38 nTPM
- midbrain: 37 nTPM
- pons: 36 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)
- 0.51
- gnomAD pLI
- 0.4
- gnomAD missense Z
- 0.61
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 15% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- UAP56-interacting factor
- Forty-two-three protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FYTTD1 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 FYTTD1 as an antibody target. Whether an autoantibody or antibody against FYTTD1 could matter depends on whether native FYTTD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FYTTD1 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 FYTTD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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