FUT9
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9
Also known as: Fuc-TIX, FUT9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y231
- Gene
- FUT9
- Ensembl
- ENSG00000172461
- Chromosome
- 6
- Canonical length
- 359 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Microtubules,Cytokinetic bridge,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The protein encoded by this gene belongs to the glycosyltransferase family. It is localized to the golgi, and catalyzes the last step in the biosynthesis of Lewis X (LeX) antigen, the addition of a fucose to precursor polysaccharides. This protein is one of the few fucosyltransferases that synthesizes the LeX oligosaccharide (CD15) expressed in the organ buds progressing in mesenchyma during embryogenesis. It is also responsible for the expression of CD15 in mature granulocytes. A common haplotype of this gene has also been associated with susceptibility to placental malaria infection. [provided by RefSeq, Nov 2011]
Canonical amino-acid sequenceUniProt
359 residues, UniProt reviewed canonical sequence.
>Q9Y231|FUT9
1 MTSTSKGILR PFLIVCIILG CFMACLLIYI KPTNSWIFSP MESASSVLKM KNFFSTKTDY
61 FNETTILVWV WPFGQTFDLT SCQAMFNIQG CHLTTDRSLY NKSHAVLIHH RDISWDLTNL
121 PQQARPPFQK WIWMNLESPT HTPQKSGIEH LFNLTLTYRR DSDIQVPYGF LTVSTNPFVF
181 EVPSKEKLVC WVVSNWNPEH ARVKYYNELS KSIEIHTYGQ AFGEYVNDKN LIPTISTCKF
241 YLSFENSIHK DYITEKLYNA FLAGSVPVVL GPSRENYENY IPADSFIHVE DYNSPSELAK
301 YLKEVDKNNK LYLSYFNWRK DFTVNLPRFW ESHACLACDH VKRHQEYKSV GNLEKWFWNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FUT9 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- stomach: 22 nTPM
- cerebral cortex: 16 nTPM
- cerebellum: 15 nTPM
- basal ganglia: 7.1 nTPM
- amygdala: 6.4 nTPM
- midbrain: 6.1 nTPM
Single-cell type
- mucous neck cells: 1,470 nCPM
- astrocytes: 1,172 nCPM
- bergmann glia: 649 nCPM
- gastric chief cells: 597 nCPM
- ependymal cells: 566 nCPM
- brain inhibitory neurons: 426 nCPM
Immune cell
- basophil: 0.2 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- midbrain: 65 nTPM
- thalamus: 57 nTPM
- cerebellum: 53 nTPM
- hypothalamus: 52 nTPM
- cerebral cortex: 49 nTPM
- amygdala: 46 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)
- 0.72
- gnomAD pLI
- 0.08
- gnomAD missense Z
- 2.02
- DepMap mean gene effect
- 0.16
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- carbohydrate metabolic process
- glycoprotein biosynthetic process
- glycosphingolipid biosynthetic process
- L-fucose catabolic process
- Lewis x epitope biosynthetic process
- N-glycan processing
- neuron differentiation
- neuronal stem cell division
- oligosaccharide biosynthetic process
- polysaccharide biosynthetic process
- positive regulation of neuron projection development
- protein N-linked glycosylation
- protein O-linked glycosylation
- regulation of leukocyte cell-cell adhesion
- regulation of leukocyte tethering or rolling
Molecular functions
- 4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase activity
- alpha-(1->3)-fucosyltransferase activity
- fucosyltransferase activity
- protein homodimerization activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FUT9 as an antibody target. Whether an autoantibody or antibody against FUT9 could matter depends on whether native FUT9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FUT9 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 FUT9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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