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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
xylosyltransferase 2
Summary
- Gene Symbol
-
- XYLT2
- Aliases
-
- PXYLT2
- XT-II
- protein xylosyltransferase 2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Disease variant
- Disulfide bond
- Glycoprotein
- Glycosyltransferase
- Golgi apparatus
- Magnesium
- Manganese
- Membrane
- Metal-binding
- Proteomics identification
- Reference proteome
- Secreted
- Signal-anchor
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| heparin biosynthetic process |
GO Hierarchy
biological process
metabolic process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular space | ||
| Golgi membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein xylosyltransferase activity | ||
| magnesium ion binding | ||
| manganese ion binding |
GO Hierarchy
GlycoGene Database (GGDB)
- GGDB ID
- gg170
- Gene Symbol
-
- XYLT2
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Rattus norvegicus | NP_071632 | NM_022296 |
| Caenorhabditis elegans | AAO85277 | AY241928 |
| Mus musculus | CAC185567 | AJ291751 |
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060609 | microcephalic osteodysplastic primordial dwarfism type II | |
| DOID:0060644 | chondrodysplasia-pseudohermaphroditism syndrome | |
| DOID:0060764 | autosomal recessive Robinow syndrome | |
| DOID:0060765 | autosomal dominant Robinow syndrome 2 | |
| DOID:0060766 | autosomal dominant Robinow syndrome 1 | |
| DOID:0060767 | autosomal dominant Robinow syndrome 3 | |
| DOID:0060891 | Parkinson's disease 19A | |
| DOID:0060895 | Parkinson's disease 4 | |
| DOID:0060896 | Parkinson's disease 23 | |
| DOID:0080177 | hepatic veno-occlusive disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000164 | Abnormality of the dentition |
| HP:0000233 | Thin vermilion border |
| HP:0000297 | Facial hypotonia |
| HP:0000316 | Hypertelorism |
| HP:0000343 | Long philtrum |
| HP:0000358 | Posteriorly rotated ears |
| HP:0000369 | Low-set ears |
| HP:0000391 | Thickened helices |
| HP:0000407 | Sensorineural hearing impairment |
| Disease ID | Disease Name |
|---|---|
| ORPHA:85194 |
|
| OMIM:605822 |
|
| OMIM:264800 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 217119 | MGI:2444797 | MOUSE07186 | |
| 64134 | RGD:619765 | RATNO00346 | |
| 100714934 | CAVPO17359 | ||
| 101577986 | OCTDE12396 | ||
| 113877936 | BOBOX14877 | ||
| 102011075 | CHILA12504 | ||
| 105724726 | AOTNA26373 | ||
| 101048643 | SAIBB18813 | ||
| 101961326 | ICTTR18595 | ||
| 101616710 | JACJA07092 |
