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MIRAGE
H(+)/Cl(-) exchange transporter 5
Summary
- UniProt ID
- P51795
- Gene Symbol
-
- CLCK2
- CLCN5
- Gene ID
- 1184
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P51795
- PubChem
- P51795
- The Human Metabolome Database
- HMDBP08187
- Re-Glyco
- P51795
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Alternative splicing
- Antiport
- CBS domain
- Cell membrane
- Chloride
- Disease variant
- Endosome
- Golgi apparatus
- Ion transport
- Proteomics identification
- Reference proteome
- Repeat
- Transmembrane helix
- Ubl conjugation
- Gene Ontology (GO)
| GO Term |
|---|
| plasma membrane |
| membrane |
| Golgi membrane |
| early endosome |
| Golgi apparatus |
| cytosol |
| apical part of cell |
| lysosomal membrane |
| synaptic vesicle |
| endosome membrane |
| GO Term |
|---|
| chloride transport |
| renal system process |
| endocytosis |
| monoatomic ion transmembrane transport |
| GO Term |
|---|
| antiporter activity |
| ATP binding |
| identical protein binding |
| voltage-gated chloride channel activity |
Sequence
MAMWQGAMDNRGFQQGSFSSFQNSSSDEDLMDIPATAMDFSMRDDVPPLDREVGEDKSYNGGGIGSSNRIMDFLEEPIPGVGTYDDFNTIDWVREKSRDRDRHREITNKSKESTWALIHSVSDAFSGWLLMLLIGLLSGSLAGLIDISAHWMTDLKEGICTGGFWFNHEHCCWNSEHVTFEERDKCPEWNSWSQLIISTDEGAFAYIVNYFMYVLWALLFAFLAVSLVKVFAPYACGSGIPEIKTILSGFIIRGYLGKWTLVIKTITLVLAVSSGLSLGKEGPLVHVACCCGNILCHCFNKYRKNEAKRREVLSAAAAAGVSVAFGAPIGGVLFSLEEVSYYFPLKTLWRSFFAALVAAFTLRSINPFGNSRLVLFYVEFHTPWHLFELVPFILLGIFGGLWGALFIRTNIAWCRKRKTTQLGKYPVIEVLVVTAITAILAFPNEYTRMSTSELISELFNDCGLLDSSKLCDYENRFNTSKGGELPDRPAGVGVYSAMWQLALTLILKIVITIFTFGMKIPSGLFIPSMAVGAIAGRLLGVGMEQLAYYHQEWTVFNSWCSQGADCITPGLYAMVGAAACLGGVTRMTVSLVVIMFELTGGLEYIVPLMAAAMTSKWVADALGREGIYDAHIRLNGYPFLEAKEEFAHKTLAMDVMKPRRNDPLLTVLTQDSMTVEDVETIISETTYSGFPVVVSRESQRLVGFVLRRDLIISIENARKKQDGVVSTSIIYFTEHSPPLPPYTPPTLKLRNILDLSPFTVTDLTPMEIVVDIFRKLGLRQCLVTHNGRLLGIITKKDVLKHIAQMANQDPDSILFN
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Stimuli-sensing channels | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080353 | X-linked recessive hypophosphatemic rickets | |
| DOID:0081453 | Dent disease 1 | |
| DOID:0111798 | X-linked nephrolithiasis type I | |
| DOID:0111815 | low molecular weight proteinuria with hypercalciuric nephrocalcinosis |
