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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:0111135 | congenital generalized lipodystrophy type 1 | |
| DOID:0111136 | congenital generalized lipodystrophy type 2 | |
| DOID:0111137 | congenital generalized lipodystrophy type 3 | |
| DOID:0111138 | congenital generalized lipodystrophy type 4 | |
| DOID:0111154 | postural orthostatic tachycardia syndrome | |
| DOID:0111414 | trichohepatoenteric syndrome | |
| DOID:0111415 | trichohepatoenteric syndrome 1 | |
| DOID:10003 | sensorineural hearing loss | |
| DOID:10127 | cerebral artery occlusion | |
| DOID:10375 | strabismic amblyopia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000973 | Cutis laxa |
| HP:0000974 | Hyperextensible skin |
| HP:0001004 | Lymphedema |
| HP:0001102 | Angioid streaks of the fundus |
| HP:0001166 | Arachnodactyly |
| HP:0001249 | Intellectual disability |
| HP:0001297 | Stroke |
| HP:0001324 | Muscle weakness |
| HP:0001382 | Joint hypermobility |
| HP:0001629 | Ventricular septal defect |
| 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 |
|---|---|---|---|
| 190099 | WB:WBGene00005024 | ||
| 38288 | FB:FBgn0015360 | ||
| 619275 | CIOIN06429 | ||
| 563446 | ZFIN:ZDB-GENE-081022-125 | ||
| 108701100 | Xenbase:XB-GENE-6486005 | ||
| 448400 | Xenbase:XB-GENE-993408 | ||
| 105579440 | CERAT29321 | ||
| 102133732 | MACFA13710 | ||
| 105472374 | MACNE31522 | ||
| 101013908 | PAPAN13271 |
