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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
Summary
- Gene Symbol
-
- PLOD3
- Aliases
-
- LH3
- Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3
- lysyl hydroxlase 3
- Organism
- Homo sapiens (human)
Annotation
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| in utero embryonic development | ||
| epidermis morphogenesis | ||
| collagen metabolic process |
GO Hierarchy
- collagen metabolic process
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen | ||
| endoplasmic reticulum | ||
| trans-Golgi network | ||
| endoplasmic reticulum membrane | ||
| collagen-containing extracellular matrix |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| small molecule binding | ||
| procollagen glucosyltransferase activity | ||
| iron ion binding | ||
| procollagen galactosyltransferase activity | ||
| metal ion binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:10480 | diaphragmatic eventration | |
| DOID:1107 | esophageal carcinoma | |
| DOID:11634 | myxedema | |
| DOID:11830 | myopia | |
| DOID:11836 | clubfoot | |
| DOID:1222 | cartilage disease | |
| DOID:1324 | lung cancer | |
| DOID:1325 | bronchus cancer | |
| DOID:14004 | thoracic aortic aneurysm | |
| DOID:1459 | hypothyroidism |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000926 | Platyspondyly |
| HP:0000938 | Osteopenia |
| HP:0000978 | Bruising susceptibility |
| HP:0001263 | Global developmental delay |
| HP:0001511 | Intrauterine growth retardation |
| HP:0001776 | Bilateral talipes equinovarus |
| HP:0001873 | Thrombocytopenia |
| HP:0002119 | Ventriculomegaly |
| HP:0002132 | Porencephalic cyst |
| HP:0002164 | Nail dysplasia |
| Disease ID | Disease Name |
|---|---|
| OMIM:612394 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 174564 | WB:WBGene00002497 | ||
| 39265 | FB:FBgn0036147 | ||
| 556077 | ZFIN:ZDB-GENE-021031-4 | DANRE24743 | |
| 108275691 | ICTPU07525 | ||
| 115183238 | SALTR50777 | ||
| 115529392 | GADMO20708 | ||
| 100697420 | ORENI49600 | ||
| 115589962 | SPAAU07491 | ||
| 380138 | Xenbase:XB-GENE-5916727 | ||
| 495489 | Xenbase:XB-GENE-17339835 |
