Identification |
HMDB Protein ID
| CDBP05410 |
Secondary Accession Numbers
| Not Available |
Name
| Magnesium transporter NIPA1 |
Description
| Not Available |
Synonyms
|
- Non-imprinted in Prader-Willi/Angelman syndrome region protein 1
- Spastic paraplegia 6 protein
|
Gene Name
| NIPA1 |
Protein Type
| Transporter |
Biological Properties |
General Function
| Not Available |
Specific Function
| Acts as a Mg(2+) transporter. Can also transport other divalent cations such as Fe(2+), Sr(2+), Ba(2+), Mn(2+) and Co(2+) but to a much less extent than Mg(2+) (By similarity).
|
GO Classification
|
Biological Process |
cell death |
Cellular Component |
early endosome |
integral to membrane |
plasma membrane |
Molecular Function |
magnesium ion transmembrane transporter activity |
|
Cellular Location
|
Not Available
|
Pathways
|
Not Available
|
Gene Properties |
Chromosome Location
| 15 |
Locus
| 15q11.2 |
SNPs
| Not Available |
Gene Sequence
|
Not Available
|
Protein Properties |
Number of Residues
| Not Available |
Molecular Weight
| 27309.285 |
Theoretical pI
| 7.168 |
Pfam Domain Function
|
|
Signals
|
Not Available
|
Transmembrane Regions
|
Not Available
|
Protein Sequence
|
>gi|214010179|ref|NP_001135747.1| magnesium transporter NIPA1 isoform 2 [Homo sapiens]
MAVGQIGNFLAYTAVPTVLVTPLGALGVPFGSILASYLLKEKLNILGKLGCLLSCAGSVV
LIIHSPKSES
|
External Links |
GenBank ID Protein
| Not Available |
UniProtKB/Swiss-Prot ID
| Q7RTP0 |
UniProtKB/Swiss-Prot Entry Name
| Not Available |
PDB IDs
|
Not Available |
GenBank Gene ID
| Not Available |
GeneCard ID
| Not Available |
GenAtlas ID
| Not Available |
HGNC ID
| HGNC:17043 |
References |
General References
| Not Available |