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Repository for lectin-assisted multimodality data
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MIRAGE
solute carrier family 12 member 2
Summary
- Gene Symbol
-
- SLC12A2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Cell membrane
- Chloride
- Disease variant
- Disulfide bond
- Intellectual disability
- Non-syndromic deafness
- Phosphoprotein
- Potassium transport
- Reference proteome
- Sodium transport
- Symport
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| ion transport | ||
| monoatomic ion transport | ||
| intracellular sodium ion homeostasis | ||
| cell volume homeostasis | ||
| cell volume homeostasis |
GO Hierarchy
biological process
cellular process [inference]
homeostatic process [inference]
response to stimulus [inference]
localization [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell body membrane | ||
| extracellular exosome | ||
| cell periphery | ||
| cell periphery | ||
| extracellular vesicle |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| sodium:potassium:chloride symporter activity | ||
| sodium:potassium:chloride symporter activity | ||
| sodium:potassium:chloride symporter activity | ||
| ammonium transmembrane transporter activity |
GO Hierarchy
molecular function
transporter activity [inference]
transmembrane transporter activity [inference]
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- solute carrier family 12 member
- Functional Category
-
- E: Amino acid transport and metabolism
- K: Transcription
- M: Cell wall/membrane/envelope biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| cell volume homeostasis |
| chloride ion homeostasis |
| chloride transmembrane transport |
| chloride |
| monoatomic ion transport |
| potassium ion homeostasis |
| InterPro |
|---|
| Amino acid permease/ SLC12A domain |
| SLC12A transporter family |
| SLC12A transporter, C-terminal |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0112159 | autosomal dominant nonsyndromic deafness 78 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 6557 | FB:FBgn0036279 | ||
| 6558 | Xenbase:XB-GENE-865887 | ||
| 6559 | FB:FBgn0036279 | ||
| 20495 | FB:FBgn0036279 | ||
| 20496 | ZFIN:ZDB-GENE-040625-53 | MOUSE23239 | |
| 20497 | FB:FBgn0036279 | ||
| 54300 | FB:FBgn0036279 | ||
| 83629 | RATNO13263 | ||
| 415170 | ZFIN:ZDB-GENE-040625-53 | DANRE00284 | |
| 471620 | PANTR36063 |
