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Repository for lectin-assisted multimodality data
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MIRAGE
Organic cation/carnitine transporter 2
Summary
- UniProt ID
- O76082
- Gene Symbol
-
- OCTN2
- SLC22A5
- Gene ID
- 6584
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- O76082
- PubChem
- O76082
- The Human Metabolome Database
- HMDBP01612
- Re-Glyco
- O76082
Annotation
- Keyword
-
- ATP-binding
- Alternative splicing
- Cell membrane
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Phosphoprotein
- Reference proteome
- Sodium transport
- Symport
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| cytoplasm |
| plasma membrane |
| endoplasmic reticulum |
| cytosol |
| basal plasma membrane |
| apical plasma membrane |
| brush border membrane |
| extracellular exosome |
Sequence
MRDYDEVTAFLGEWGPFQRLIFFLLSASIIPNGFTGLSSVFLIATPEHRCRVPDAANLSSAWRNHTVPLRLRDGREVPHSCRRYRLATIANFSALGLEPGRDVDLGQLEQESCLDGWEFSQDVYLSTIVTEWNLVCEDDWKAPLTISLFFVGVLLGSFISGQLSDRFGRKNVLFVTMGMQTGFSFLQIFSKNFEMFVVLFVLVGMGQISNYVAAFVLGTEILGKSVRIIFSTLGVCIFYAFGYMVLPLFAYFIRDWRMLLVALTMPGVLCVALWWFIPESPRWLISQGRFEEAEVIIRKAAKANGIVVPSTIFDPSELQDLSSKKQQSHNILDLLRTWNIRMVTIMSIMLWMTISVGYFGLSLDTPNLHGDIFVNCFLSAMVEVPAYVLAWLLLQYLPRRYSMATALFLGGSVLLFMQLVPPDLYYLATVLVMVGKFGVTAAFSMVYVYTAELYPTVVRNMGVGVSSTASRLGSILSPYFVYLGAYDRFLPYILMGSLTILTAILTLFLPESFGTPLPDTIDQMLRVKGMKHRKTPSHTRMLKDGQERPTILKSTAF
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 57 | N-linked (GlcNAc...) asparagine | |||
| 64 | N-linked (GlcNAc...) asparagine | |||
| 91 | N-linked (GlcNAc...) asparagine |
G27058EU
G70441OD
G83460ZZ
G80920RR
G62765YT
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Carnitine shuttle | Homo sapiens |
| Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP) | Homo sapiens |
| Organic cation transport | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050700 | cardiomyopathy | |
| DOID:14365 | systemic primary carnitine deficiency disease | |
| DOID:655 | inherited metabolic disorder | |
| DOID:8778 | Crohn's disease |
