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
malonyl-CoA-acyl carrier protein transacylase
Summary
- Gene Symbol
-
- MCAT
- Aliases
-
- FASN2C
- MCT
- MCT1
- MT
- NET62
- [acyl-carrier-protein] S-malonyltransferase
- fabD
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Disease variant
- Fatty acid biosynthesis
- Mitochondrion
- Reference proteome
- Transferase
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| Q8IVS2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid beta-oxidation |
|
|
| fatty acid biosynthetic process | ||
| mitochondrial small ribosomal subunit assembly |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial matrix |
|
|
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| [acyl-carrier-protein] S-malonyltransferase activity | ||
| RNA binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050873 | follicular lymphoma | |
| DOID:0060058 | lymphoma | |
| DOID:0060060 | non-Hodgkin lymphoma | |
| DOID:0060891 | Parkinson's disease 19A | |
| DOID:0060895 | Parkinson's disease 4 | |
| DOID:0060896 | Parkinson's disease 23 | |
| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | |
| DOID:0070219 | familial hyperinsulinemic hypoglycemia 1 | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0111412 | exudative vitreoretinopathy 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000543 | Optic disc pallor |
| HP:0000603 | Central scotoma |
| HP:0000613 | Photophobia |
| HP:0000639 | Nystagmus |
| HP:0000648 | Optic atrophy |
| HP:0002315 | Headache |
| HP:0003621 | Juvenile onset |
| HP:0007641 | Dyschromatopsia |
| HP:0007663 | Reduced visual acuity |
| Disease ID | Disease Name |
|---|---|
| OMIM:620583 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001404
- Gene Name
- malonyl CoA:ACP acyltransferase (mitochondrial)
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 259414 | WB:WBGene00016812 | ||
| 39910 | FB:FBgn0036691 | ||
| 103181833 | CALMI23824 | ||
| 564111 | ZFIN:ZDB-GENE-041111-231 | DANRE34168 | |
| 103032777 | ASTMX16092 | ||
| 108280020 | ICTPU12715 | ||
| 113572509 | ELEEL12249 | ||
| 115180574 | SALTR55253 | ||
| 115199068 | SALTR64939 | ||
| 115532379 | GADMO24258 |
