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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
aralar1
Summary
- Gene Symbol
-
- aralar1
- Organism
- Drosophila melanogaster (fruit fly)
Annotation
- Keyword
-
- Alternative splicing
- Calcium
- Metal-binding
- Mitochondrion inner membrane
- Proteomics identification
- Reference proteome
- Repeat
- Transmembrane helix
- Transport
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9VA73 |
|
| A0A0B4KHW3 |
|
| A0A0B4K6V1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| L-aspartate transmembrane transport | ||
| malate-aspartate shuttle | ||
| wound healing | ||
| L-glutamate transmembrane transport | ||
| gluconeogenesis |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial inner membrane | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| gamma-aminobutyric acid:proton symporter activity | ||
| L-glutamate transmembrane transporter activity | ||
| identical protein binding | ||
| L-aspartate transmembrane transporter activity | ||
| aspartate:glutamate, proton antiporter activity |
GO Hierarchy
molecular function
transporter activity [inference]
transmembrane transporter activity [inference]
organic acid transmembrane transporter activity [inference]
organic anion transmembrane transporter activity [inference]
monoatomic ion transmembrane transporter activity [inference]
active transmembrane transporter activity [inference]
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Mitochondrial carrier protein, calcium-binding
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| L-aspartate transmembrane transporter activity |
| L-glutamate transmembrane transporter activity |
| calcium ion binding |
| malate-aspartate shuttle |
Alliance of Genome Resources
- Expression
| Location | References |
|---|---|
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050432 | Asperger syndrome | |
| DOID:0050696 | fetal alcohol spectrum disorder | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0070341 | neonatal-onset type II citrullinemia | |
| DOID:0070342 | adult-onset type II citrullinemia | |
| DOID:0080349 | developmental and epileptic encephalopathy 39 | |
| DOID:12849 | autistic disorder | |
| DOID:1852 | intrahepatic cholestasis | |
| DOID:4137 | common bile duct disease | |
| DOID:9273 | citrullinemia |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 108156662 | 7229_0:001760 | |||
| 108604370 | 30019_1:0021da | |||
| 108621351 | 7263_0:000962 | |||
| 108656834 | 7232_1:000edb | |||
| 110186616 | 7274_0:0029d6 | |||
| 111066590 | 7282_0:000543 | |||
| 111592461 | 7224_1:000bf9 | |||
| 115759509 | 47314_0:000f73 | |||
| 117144301 | 7226_1:0023a3 | |||
| 117574696 | 7291_1:002a74 |
