Entry |
|
Symbol |
NIPA1, SLC57A1
|
Name |
magnesium transporter NIPA1
|
Disease |
H00266 | Hereditary spastic paraplegia |
|
Brite |
KEGG Orthology (KO) [BR:ko00001]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters
K19364 NIPA1, SLC57A1; magnesium transporter NIPA1
Transporters [BR:ko02000]
Solute carrier family (SLC)
SLC57: NiPA-like magnesium transporter
K19364 NIPA1, SLC57A1; magnesium transporter NIPA1
|
Other DBs |
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Genes |
» show all
|
Reference |
|
Authors |
Goytain A, Hines RM, El-Husseini A, Quamme GA |
Title |
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter. |
Journal |
|
Sequence |
|
Reference |
|
Authors |
Quamme GA |
Title |
Molecular identification of ancient and modern mammalian magnesium transporters. |
Journal |
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