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MIRAGE
Sodium/potassium/calcium exchanger 4
Summary
- UniProt ID
- Q8NFF2
- Gene Symbol
-
- NCKX4
- SLC24A4
- Gene ID
- 123041
- Organism
- Homo sapiens (human)
External Links
- PubChem
- Q8NFF2
- The Human Metabolome Database
- HMDBP03054
- Re-Glyco
- Q8NFF2
Annotation
- Keyword
-
- Alternative splicing
- Amelogenesis imperfecta
- Antiport
- Calcium transport
- Cell membrane
- Cytoplasm
- Disease variant
- Glycoprotein
- Olfaction
- Potassium transport
- Reference proteome
- Repeat
- Signal
- Sodium transport
- Symport
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| cytoplasm |
| plasma membrane |
| vesicle |
| membrane |
| apical plasma membrane |
| cone photoreceptor outer segment |
| GO Term |
|---|
| calcium, potassium:sodium antiporter activity |
| calcium channel activity |
| calmodulin binding |
| symporter activity |
| calcium-dependent protein binding |
Sequence
MALRGTLRPLKVRRRREMLPQQVGFVCAVLALVCCASGLFGSLGHKTASASKRVLPDTWRNRKLMAPVNGTQTAKNCTDPAIHEFPTDLFSNKERQHGAVLLHILGALYMFYALAIVCDDFFVPSLEKICERLHLSEDVAGATFMAAGSSTPELFASVIGVFITHGDVGVGTIVGSAVFNILCIIGVCGLFAGQVVRLTWWAVCRDSVYYTISVIVLIVFIYDEQIVWWEGLVLIILYVFYILIMKYNVKMQAFFTVKQKSIANGNPVNSELEAGNDFYDGSYDDPSVPLLGQVKEKPQYGKNPVVMVDEIMSSSPPKFTFPEAGLRIMITNKFGPRTRLRMASRIIINERQRLINSANGVSSKPLQNGRHENIENGNVPVENPEDPQQNQEQQPPPQPPPPEPEPVEADFLSPFSVPEARGDKVKWVFTWPLIFLLCVTIPNCSKPRWEKFFMVTFITATLWIAVFSYIMVWLVTIIGYTLGIPDVIMGITFLAAGTSVPDCMASLIVARQGLGDMAVSNTIGSNVFDILVGLGVPWGLQTMVVNYGSTVKINSRGLVYSVVLLLGSVALTVLGIHLNKWRLDRKLGVYVLVLYAIFLCFSIMIEFNVFTFVNLPMCREDD
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI) | Homo sapiens |
| Sodium/Calcium exchangers | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110063 | amelogenesis imperfecta hypomaturation type 2A5 | |
| DOID:10123 | pigmentation disease |
