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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
solute carrier family 33 member 1
Summary
- Gene Symbol
-
- SLC33A1
- Aliases
-
- AT-1
- AT1
- Acetyl-CoA transporter 1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cataract
- Deafness
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Hereditary spastic paraplegia
- Phosphoprotein
- Reference proteome
- Transmembrane helix
- Transport
- Proteins
| UniProt | Protein Name |
|---|---|
| O00400 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| transmembrane transport |
|
|
| acetyl-CoA transmembrane transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum membrane | ||
| plasma membrane |
|
|
| membrane | ||
| Golgi membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein homodimerization activity | ||
| acetyl-CoA transmembrane transporter activity | ||
| protein binding |
GO Hierarchy
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:0080348 | Alzheimer's disease 1 | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 | |
| DOID:0110038 | Alzheimer's disease 6 | |
| DOID:0110039 | Alzheimer's disease 7 | |
| DOID:0110041 | Alzheimer's disease 8 | |
| DOID:0110043 | Alzheimer's disease 10 | |
| DOID:0110044 | Alzheimer's disease 11 | |
| DOID:0110045 | Alzheimer's disease 12 | |
| DOID:0110046 | Alzheimer's disease 13 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000365 | Hearing impairment |
| HP:0000519 | Developmental cataract |
| HP:0000639 | Nystagmus |
| HP:0001250 | Seizure |
| HP:0001252 | Hypotonia |
| HP:0001258 | Spastic paraplegia |
| HP:0001272 | Cerebellar atrophy |
| HP:0001324 | Muscle weakness |
| Disease ID | Disease Name |
|---|---|
| OMIM:614482 |
|
| OMIM:612539 |
|
| ORPHA:171863 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP004676
- Gene Name
- solute carrier family 33 (acetyl-CoA transporter), member 1
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 259455 | WB:WBGene00012033 | ||
| 39876 | FB:FBgn0036662 | ||
| 100181010 | CIOIN10390 | ||
| 103175692 | CALMI00032 | ||
| 102354281 | LATCH19439 | ||
| 394083 | ZFIN:ZDB-GENE-040426-1241 | DANRE14687 | |
| 103040971 | ASTMX14661 | ||
| 108264671 | ICTPU28819 | ||
| 113589428 | ELEEL42988 | ||
| 115163756 | SALTR97880 |
