KEGG   Homo sapiens (human): 123606
Entry
123606            CDS       T01001                                 
Symbol
NIPA1, FSP3, SLC57A1, SPG6
Name
(RefSeq) NIPA magnesium transporter 1
  KO
K19364  magnesium transporter NIPA1
Organism
hsa  Homo sapiens (human)
Disease
H00266  Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    123606 (NIPA1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC57: NiPA-like magnesium transporter
   123606 (NIPA1)
SSDB
Motif
Pfam: Mg_trans_NIPA EamA
Other DBs
NCBI-GeneID: 123606
NCBI-ProteinID: NP_653200
OMIM: 608145
HGNC: 17043
Ensembl: ENSG00000170113
UniProt: Q7RTP0
Position
15:22786225..22829789
AA seq 329 aa
MGTAAAAAAAAAAAAAGEGARSPSPAAVSLGLGVAVVSSLVNGSTFVLQKKGIVRAKRRG
TSYLTDIVWWAGTIAMAVGQIGNFLAYTAVPTVLVTPLGALGVPFGSILASYLLKEKLNI
LGKLGCLLSCAGSVVLIIHSPKSESVTTQAELEEKLTNPVFVGYLCIVLLMLLLLIFWIA
PAHGPTNIMVYISICSLLGSFTVPSTKGIGLAAQDILHNNPSSQRALCLCLVLLAVLGCS
IIVQFRYINKALECFDSSVFGAIYYVVFTTLVLLASAILFREWSNVGLVDFLGMACGFTT
VSVGIVLIQVFKEFNFNLGEMNKSNMKTD
NT seq 990 nt   +upstreamnt  +downstreamnt
atggggactgcagctgcggcagcggcggcggcggcggcggcggcggccggggagggggcg
cgtagcccgagccccgccgccgtgtcgctcggcctgggcgtggccgtcgtgtcgagcctg
gtgaacgggtccacgttcgtgctacagaagaagggcatcgtgcgtgccaagcggcgaggt
acttcctatttaacagacattgtgtggtgggctggcacaatcgcaatggctgttggccag
attggaaacttcctggcttacacggcggtccccacggtcctggtaacccccctgggcgcc
cttggagtaccgttcgggtccattttagcttcctatctcctgaaggaaaagctcaacatc
ttgggcaagttggggtgcctgctaagctgtgcaggctccgtcgtgctgattatccactcc
ccaaagtctgagagtgtgacaactcaggctgagctggaggaaaagctgaccaatccagtg
tttgtgggctacctgtgcatcgtgctgctcatgctgctgctgctcatcttctggatcgcg
ccggcccatgggcccaccaacatcatggtctacatcagcatctgctccttgctgggcagt
ttcaccgtgccttccaccaagggcatcgggctggcggcccaagacatcttgcataacaac
ccgtccagtcagagagccctctgcctgtgcctggtactcctggccgtgctcggctgcagc
atcatcgtccagttcaggtacatcaacaaggcgctggagtgcttcgactcctcggtgttc
ggggccatctactacgtcgtgtttaccacgctggtcctgctggcctcagccatcctcttc
cgggagtggagcaacgtgggcctggtggacttcttggggatggcctgtggattcacgacc
gtctccgtggggattgtccttatacaggtgttcaaagagttcaatttcaaccttggggag
atgaacaaatctaatatgaaaacagactag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (8)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (16)   
   RefSeq(nuc) (2)   
   GenBank (7)   
   EMBL (7)   
Protein domain (2)   
   Pfam (2)   
All databases (36)   

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