Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
leukotriene C4 synthase
Summary
- Gene Symbol
-
- LTC4S
- Aliases
-
- MGC33147
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Direct protein sequencing
- Endoplasmic reticulum
- Leukotriene biosynthesis
- Lipid biosynthesis
- Lyase
- Nucleus
- Phosphoprotein
- Reference proteome
- Transferase
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q16873 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| leukotriene biosynthetic process | ||
| leukotriene metabolic process | ||
| long-chain fatty acid biosynthetic process | ||
| cellular oxidant detoxification |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nuclear envelope | ||
| intracellular membrane-bounded organelle |
|
|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| nuclear outer membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| lipid binding | ||
| glutathione peroxidase activity | ||
| leukotriene-C4 synthase activity | ||
| enzyme activator activity | ||
| protein binding |
GO Hierarchy
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:1558 | angioedema | |
| DOID:2237 | hepatitis | |
| DOID:224 | transient cerebral ischemia | |
| DOID:2320 | obstructive lung disease | |
| DOID:2452 | thrombophilia | |
| DOID:2841 | asthma | |
| DOID:2921 | glomerulonephritis | |
| DOID:2935 | Chediak-Higashi syndrome | |
| DOID:3083 | chronic obstructive pulmonary disease | |
| DOID:3393 | coronary artery disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000252 | Microcephaly |
| HP:0001252 | Hypotonia |
| HP:0001263 | Global developmental delay |
| HP:0001522 | Death in infancy |
| HP:0001531 | Failure to thrive in infancy |
| Disease ID | Disease Name |
|---|---|
| OMIM:614037 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002479
- Gene Name
- leukotriene C4 synthase
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 112932405 | VULVU28215 | ||
| 101681631 | MUSPF10709 | ||
| 101096198 | FELCA01091 | ||
| 122216164 | PANLE12648 | ||
| 101329342 | TURTR00729 | ||
| 118892932 | BALMU07106 | ||
| 100675058 | LOXAF20381 | ||
| 100520063 | PIGXX19090 | ||
| 511749 | BOVIN32046 | ||
| 106502247 | CAPHI28628 |
