Gene

xylt1.L

Species
Xenopus laevis
Symbol
xylt1.L
Name
xylosyltransferase I
Synonyms
  • xylosyltransferase I
  • xylt1.L
Biotype
gene
Automated Description
Predicted to enable metal ion binding activity and protein xylosyltransferase activity. Predicted to act upstream of or within chondroitin sulfate biosynthetic process and heparan sulfate proteoglycan biosynthetic process. Predicted to be located in Golgi membrane. Human ortholog(s) of this gene implicated in Desbuquois dysplasia; pseudoxanthoma elasticum; and type 1 diabetes mellitus. Orthologous to human XYLT1 (xylosyltransferase 1).
XBXL Description
Cross References
Additional Information
Literature

Orthology

Gene tree
Not Available
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
XL9.2
Viewer Help
92.16M92.18M92.20M92.22M92.24M92.26M92.28M92.30M92.32M92.34M

Sequence Details

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Expression

Primary Sources
Other Sources
None
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions