Organism | UniProt | Comment | Textmining |
---|---|---|---|
Bos taurus | A4IFH1 | - |
- |
Bos taurus | Q28113 | - |
- |
Bos taurus | Q9TTY3 | - |
- |
Chlorocebus sabaeus | - |
- |
- |
Chlorocebus sabaeus | O77711 | - |
- |
Chlorocebus sabaeus | O77712 | - |
- |
Gorilla gorilla | O77486 | - |
- |
Gorilla gorilla | Q9TUD4 | - |
- |
Homo sapiens | P19526 | - |
- |
Homo sapiens | Q10981 | - |
- |
Homo sapiens | Q5XLR8 | - |
- |
Hylobates agilis | Q6LA46 | - |
- |
Hylobates lar | Q9TTC7 | - |
- |
Macaca fascicularis | Q9N266 | fragment | - |
Monodelphis domestica | - |
a FUT2-like gene sequence in opossum is found | - |
Mus musculus | O09160 | - |
- |
Mus musculus | P97353 | - |
- |
Oryctolagus cuniculus | Q10979 | - |
- |
Oryctolagus cuniculus | Q10983 | - |
- |
Oryctolagus cuniculus | Q29505 | - |
- |
Pan troglodytes | O77485 | - |
- |
Pan troglodytes | Q9TUD6 | - |
- |
Pongo pygmaeus | O77487 | - |
- |
Pongo pygmaeus | Q6LA45 | - |
- |
Rattus norvegicus | Q10980 | - |
- |
Rattus norvegicus | Q10984 | - |
- |
Rattus norvegicus | Q9WUE6 | - |
- |
Sus scrofa | Q10982 | - |
- |
Sus scrofa | Q29043 | - |
- |
Xenopus tropicalis | - |
- |
- |
Synonyms | Comment | Organism |
---|---|---|
alpha-2-fucosyltransferase | - |
Chlorocebus sabaeus |
alpha-2-fucosyltransferase | - |
Homo sapiens |
alpha-2-fucosyltransferase | - |
Xenopus tropicalis |
alpha-2-fucosyltransferase | - |
Pongo pygmaeus |
alpha-2-fucosyltransferase | - |
Hylobates lar |
alpha-2-fucosyltransferase | - |
Hylobates agilis |
alpha-2-fucosyltransferase | - |
Macaca fascicularis |
alpha-2-fucosyltransferase | - |
Bos taurus |
alpha-2-fucosyltransferase | - |
Mus musculus |
alpha-2-fucosyltransferase | - |
Rattus norvegicus |
alpha-2-fucosyltransferase | - |
Sus scrofa |
alpha-2-fucosyltransferase | - |
Oryctolagus cuniculus |
alpha-2-fucosyltransferase | - |
Pan troglodytes |
alpha-2-fucosyltransferase | - |
Gorilla gorilla |
alpha1,2fucosyltransferase | - |
Chlorocebus sabaeus |
alpha1,2fucosyltransferase | - |
Homo sapiens |
alpha1,2fucosyltransferase | - |
Xenopus tropicalis |
alpha1,2fucosyltransferase | - |
Pongo pygmaeus |
alpha1,2fucosyltransferase | - |
Hylobates lar |
alpha1,2fucosyltransferase | - |
Hylobates agilis |
alpha1,2fucosyltransferase | - |
Macaca fascicularis |
alpha1,2fucosyltransferase | - |
Bos taurus |
alpha1,2fucosyltransferase | - |
Mus musculus |
alpha1,2fucosyltransferase | - |
Rattus norvegicus |
alpha1,2fucosyltransferase | - |
Sus scrofa |
alpha1,2fucosyltransferase | - |
Oryctolagus cuniculus |
alpha1,2fucosyltransferase | - |
Pan troglodytes |
alpha1,2fucosyltransferase | - |
Gorilla gorilla |
alpha2FT | - |
Chlorocebus sabaeus |
alpha2FT | - |
Homo sapiens |
alpha2FT | - |
Xenopus tropicalis |
alpha2FT | - |
Pongo pygmaeus |
alpha2FT | - |
Hylobates lar |
alpha2FT | - |
Hylobates agilis |
alpha2FT | - |
Macaca fascicularis |
alpha2FT | - |
Bos taurus |
alpha2FT | - |
Mus musculus |
alpha2FT | - |
Rattus norvegicus |
alpha2FT | - |
Sus scrofa |
alpha2FT | - |
Oryctolagus cuniculus |
alpha2FT | - |
Pan troglodytes |
alpha2FT | - |
Gorilla gorilla |
FUT1 | - |
Homo sapiens |
FUT1 | - |
Xenopus tropicalis |
FUT1 | - |
Chlorocebus sabaeus |
FUT1 | - |
Bos taurus |
FUT1 | - |
Mus musculus |
FUT1 | - |
Rattus norvegicus |
FUT1 | - |
Sus scrofa |
FUT1 | - |
Oryctolagus cuniculus |
FUT1 | - |
Pan troglodytes |
FUT1 | - |
Gorilla gorilla |
FUT2 | - |
Hylobates lar |
FUT2 | - |
Chlorocebus sabaeus |
FUT2 | - |
Bos taurus |
FUT2 | - |
Rattus norvegicus |
FUT2 | - |
Sus scrofa |
FUT2 | - |
Oryctolagus cuniculus |
FUT2 | - |
Pan troglodytes |
FUT2 | - |
Pongo pygmaeus |
FUT2 | - |
Gorilla gorilla |
FUT2 | - |
Monodelphis domestica |
FUT2 | a FUT2-like gene sequence in opossum is found | Monodelphis domestica |
Sec1 | - |
Chlorocebus sabaeus |
Sec1 | - |
Pongo pygmaeus |
Sec1 | - |
Homo sapiens |
Sec1 | - |
Hylobates agilis |
Sec1 | - |
Macaca fascicularis |
Sec1 | - |
Bos taurus |
Sec1 | - |
Mus musculus |
Sec1 | - |
Rattus norvegicus |
Sec1 | - |
Sus scrofa |
Sec1 | - |
Oryctolagus cuniculus |
General Information | Comment | Organism |
---|---|---|
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Chlorocebus sabaeus |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Xenopus tropicalis |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Hylobates lar |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Hylobates agilis |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Macaca fascicularis |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Bos taurus |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Mus musculus |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Rattus norvegicus |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Sus scrofa |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Oryctolagus cuniculus |
physiological function | Biosynthesis of cell surface glycoconjugates, which play a role in infections. For example, nonsecretors are known to be virtually resistant to infection by norovirus. Inversely, women with the nonsecretor phenotype are more prone to Escherichia coli mediated recurrent urinary tract infections than secretor women. | Gorilla gorilla |