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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:1425 | pyoureter | |
| DOID:1432 | blindness | |
| DOID:0050427 | xeroderma pigmentosum | |
| DOID:0050458 | juvenile myelomonocytic leukemia | |
| DOID:0050569 | Seckel syndrome | |
| DOID:0050778 | Meckel syndrome | |
| DOID:0060254 | Robinow syndrome | |
| DOID:0060262 | gallbladder disease | |
| DOID:0060462 | Desbuquois dysplasia | |
| DOID:0060578 | Noonan syndrome 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0004417 | Intermittent claudication |
| HP:0004467 | Preauricular pit |
| HP:0004943 | Accelerated atherosclerosis |
| HP:0005108 | Abnormal intervertebral disk morphology |
| HP:0005176 | Dysplastic aortic valve |
| HP:0007663 | Reduced visual acuity |
| HP:0007730 | Iris hypopigmentation |
| HP:0007787 | Posterior subcapsular cataract |
| HP:0008063 | Aplasia/Hypoplasia of the lens |
| HP:0009738 | Abnormal antihelix morphology |
| 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 |
|---|---|---|---|
| 102440255 | MYOLU15916 | ||
| 117013516 | RHIFE08371 | ||
| 103242938 | CHLSB05585 | ||
| 108516436 | RHIBE12508 | ||
| 104680299 | RHIRO29253 | ||
| 100600245 | NOMLE08181 | ||
| 106826421 | EQUAS21325 | ||
| 105295404 | PTEVA08002 | ||
| 105824761 | PROCO10236 | ||
| 103738383 | NANGA01344 |
