FUT6 (fucosyltransferase 6)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 2528 |
| Gene name | Fucosyltransferase 6 |
| Gene symbol | FUT6 |
| Synonyms (NCBI Gene) |
FCT3AFT1AFuc-TVIFucT-VI
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| Chromosome | 19 |
| Chromosome location | 19p13.3 |
| Summary | The protein encoded by this gene is a Golgi stack membrane protein that is involved in the creation of sialyl-Lewis X, an E-selectin ligand. Mutations in this gene are a cause of fucosyltransferase-6 deficiency. Two transcript variants encoding the same p |
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miRNA
miRNA information provided by mirtarbase database.
173
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P51993 | |||||||||||||||
| Protein name | 4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6 (EC 2.4.1.152) (Fucosyltransferase 6) (Fucosyltransferase VI) (Fuc-TVI) (FucT-VI) (Galactoside 3-L-fucosyltransferase) | |||||||||||||||
| Protein function | [Isoform 1]: Catalyzes the transfer of L-fucose, from a guanosine diphosphate-beta-L-fucose, to the N-acetyl glucosamine (GlcNAc) of a distal alpha2,3 sialylated lactosamine unit of a glycoprotein- or a glycolipid-linked sialopolylactosamines ch | |||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Kidney, liver, colon, small intestine, bladder, uterus and salivary gland. | |||||||||||||||
| Sequence |
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| Sequence length | 359 | |||||||||||||||
| Interactions | View interactions | |||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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