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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
sterol carrier protein 2
Summary
- Gene Symbol
-
- SCP2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Acyltransferase
- Alternative promoter usage
- Alternative splicing
- Cytoplasm
- Direct protein sequencing
- Endoplasmic reticulum
- Lipid metabolism
- Lipid transport
- Lipid-binding
- Mitochondrion
- Peroxisome
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A384NY87 |
|
| P22307 |
|
| B2R761 |
|
| E9PLD1 |
|
| Q59HG9 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| intracellular cholesterol transport | ||
| fatty acid beta-oxidation using acyl-CoA oxidase |
|
|
| lipid hydroperoxide transport | ||
| bile acid biosynthetic process |
|
|
| alpha-linolenic acid metabolic process |
|
GO Hierarchy
biological process
metabolic process [inference]
cellular metabolic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of localization [inference]
regulation of transport [inference]
regulation of cellular localization [inference]
regulation of lipid localization [inference]
positive regulation of biological process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| cytosol |
|
|
| membrane | ||
| peroxisome | ||
| protein-containing complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| propanoyl-CoA C-acyltransferase activity | ||
| fatty-acyl-CoA binding | ||
| acetyl-CoA C-acyltransferase activity | ||
| acetyl-CoA C-myristoyltransferase activity | ||
| oleic acid binding |
GO Hierarchy
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:0050444 | infantile Refsum disease | |
| DOID:0050646 | distal arthrogryposis | |
| DOID:0050835 | generalized dystonia | |
| DOID:0050841 | focal hand dystonia | |
| DOID:0060868 | leukoencephalopathy with vanishing white matter | |
| DOID:0080001 | bone disease | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 | |
| DOID:0110038 | Alzheimer's disease 6 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000027 | Azoospermia |
| HP:0000365 | Hearing impairment |
| HP:0000473 | Torticollis |
| HP:0000514 | Slow saccadic eye movements |
| HP:0000815 | Hypergonadotropic hypogonadism |
| HP:0001332 | Dystonia |
| HP:0002080 | Intention tremor |
| HP:0002346 | Head tremor |
| HP:0002352 | Leukoencephalopathy |
| Disease ID | Disease Name |
|---|---|
| OMIM:613724 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001075
- Gene Name
- sterol carrier protein 2
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 174881 | WB:WBGene00013284 | ||
| 35140 | FB:FBgn0032715 | ||
| 44183 | FB:FBgn0015808 | ||
| 102694821 | LEPOC01460 | ||
| 393839 | ZFIN:ZDB-GENE-040426-1846 | DANRE29605 | |
| 450073 | ZFIN:ZDB-GENE-041010-196 | ||
| 103022159 | ASTMX06475 | ||
| 108267621 | ICTPU32276 | ||
| 113570128 | ELEEL09123 | ||
| 106569705 | SALSA72470 |
