Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|
| response to bacterium | ||
| carbohydrate transmembrane transport | ||
| neurotransmitter loading into synaptic vesicle | ||
| monoatomic ion transport | ||
| amino acid transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| synaptic vesicle membrane | ||
| membrane | ||
| plasma membrane | ||
| lysosome | ||
| basolateral plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbohydrate:proton symporter activity | ||
| D-glucuronate transmembrane transporter activity | ||
| sialic acid:proton symporter activity | ||
| sialic acid transmembrane transporter activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- transporter
- 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
- 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 | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 100708225 | ORENI12067 | |||
| 100714527 | CAVPO03277 | |||
| 100757887 | CRIGR11015 | |||
| 100977861 | 9597_0:001af8 | PANPA34744 | ||
| 101074777 | TAKRU40214 | |||
| 101147234 | 9595_0:002098 | GORGO37188 | ||
| 101165833 | ORYLA04743 | |||
| 101605715 | JACJA12076 | |||
| 101808018 | FICAL09659 | |||
| 101878986 | MELUD02003 |
