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Repository for lectin-assisted multimodality data
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MIRAGE
solute carrier family 17 member 5
Summary
- Gene Symbol
-
- SLC17A5
- Aliases
-
- AST
- ISSD
- NSD
- SD
- SIALIN
- SLD
- Salla disease
- acidic sugar transporter
- infantile sialic acid storage disorder
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Amino-acid transport
- Cell membrane
- Cytoplasmic vesicle
- Disease variant
- Glycoprotein
- Lysosome
- Phosphoprotein
- Reference proteome
- Symport
- Synapse
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9NRA2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| monoatomic ion transport | ||
| ion transport | ||
| anion transport | ||
| monoatomic anion transport | ||
| amino acid transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| glutamatergic synapse |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbohydrate:proton symporter activity | ||
| sialic acid transmembrane transporter activity | ||
| sialic acid transmembrane transporter activity | ||
| sialic acid:proton symporter activity | ||
| D-glucuronate transmembrane transporter activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- mfs
- Functional Category
-
- C: Energy production and conversion
- E: Amino acid transport and metabolism
- T: Signal transduction mechanisms
| InterPro |
|---|
| MFS transporter superfamily |
| Major facilitator superfamily domain |
| Major facilitator superfamily |
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:3659 | sialuria |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000100 | Nephrotic syndrome |
| HP:0000212 | Gingival overgrowth |
| HP:0000218 | High palate |
| HP:0000238 | Hydrocephalus |
| HP:0000280 | Coarse facial features |
| HP:0000286 | Epicanthus |
| HP:0000463 | Anteverted nares |
| HP:0000508 | Ptosis |
| HP:0000577 | Exotropia |
| Disease ID | Disease Name |
|---|---|
| OMIM:269920 |
|
| OMIM:604369 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115055362 | ECHNA09754 | ||
| 115193799 | SALTR90675 | ||
| 115399774 | SALFA53574 | ||
| 115596765 | SPAAU10810 | ||
| 115609552 | STRHB17045 | ||
| 116442147 | CORMO19064 | ||
| 116815596 | CHEAB16427 | ||
| 117020563 | RHIFE11435 | ||
| 118905490 | BALMU27533 | ||
| 123796345 | URSAM10309 |
