Solute carrier family 24 member 5
GPTKB entity
Statements (17)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
|
| gptkbp:alternativeName |
gptkb:NCKX5
|
| gptkbp:associatedWith |
skin pigmentation
Oculocutaneous albinism type 6 |
| gptkbp:expressedIn |
gptkb:melanocytes
|
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
potassium-dependent sodium/calcium exchanger
cation exchange |
| gptkbp:gene |
gptkb:SLC24A5
|
| https://www.w3.org/2000/01/rdf-schema#label |
Solute carrier family 24 member 5
|
| gptkbp:locatedIn |
gptkb:human_chromosome_15
|
| gptkbp:mutationAssociatedWith |
affects melanin production
|
| gptkbp:OMIM |
609802
|
| gptkbp:orthologInMouse |
gptkb:Slc24a5
|
| gptkbp:UniProtID |
Q6TGU1
|
| gptkbp:bfsParent |
gptkb:SLC24A5
|
| gptkbp:bfsLayer |
8
|