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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
propionyl-CoA carboxylase subunit beta
Summary
- Gene Symbol
-
- PCCB
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Acetylation
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Ligase
- Mitochondrion
- Phosphoprotein
- Reference proteome
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| P05166 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid metabolic process |
|
|
| branched-chain amino acid metabolic process |
|
|
| short-chain fatty acid catabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol |
|
|
| catalytic complex | ||
| mitochondrial matrix | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| propionyl-CoA carboxylase activity | ||
| ATP binding | ||
| protein binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0050590 | severe congenital neutropenia | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0060270 | pontocerebellar hypoplasia type 2D | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0110425 | dilated cardiomyopathy 1A | |
| DOID:1059 | intellectual disability | |
| DOID:11476 | osteoporosis | |
| DOID:11832 | visual epilepsy | |
| DOID:11984 | hypertrophic cardiomyopathy |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000939 | Osteoporosis |
| HP:0000964 | Eczematoid dermatitis |
| HP:0001249 | Intellectual disability |
| HP:0001250 | Seizure |
| HP:0001254 | Lethargy |
| HP:0001259 | Coma |
| HP:0001263 | Global developmental delay |
| HP:0001332 | Dystonia |
| HP:0001508 | Failure to thrive |
| Disease ID | Disease Name |
|---|---|
| ORPHA:35 |
|
| OMIM:606054 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000406
- Gene Name
- propionyl CoA carboxylase, beta polypeptide
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 180596 | WB:WBGene00018701 | ||
| 102364951 | LATCH16877 | ||
| 405861 | ZFIN:ZDB-GENE-040426-2467 | DANRE29231 | |
| 103029063 | ASTMX03195 | ||
| 108278028 | ICTPU09668 | ||
| 113576466 | ELEEL18573 | ||
| 106574468 | SALSA83774 | ||
| 106575421 | SALSA85265 | ||
| 115183341 | SALTR50905 | ||
| 115196214 | SALTR95079 |
