Homo sapiens (human): 123606
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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)
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Gene cluster
GFIT
Motif
Pfam:
Mg_trans_NIPA
EamA
Motif
Other DBs
NCBI-GeneID:
123606
NCBI-ProteinID:
NP_653200
OMIM:
608145
HGNC:
17043
Ensembl:
ENSG00000170113
UniProt:
Q7RTP0
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Position
15:22786225..22829789
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AA seq
329 aa
AA seq
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MGTAAAAAAAAAAAAAGEGARSPSPAAVSLGLGVAVVSSLVNGSTFVLQKKGIVRAKRRG
TSYLTDIVWWAGTIAMAVGQIGNFLAYTAVPTVLVTPLGALGVPFGSILASYLLKEKLNI
LGKLGCLLSCAGSVVLIIHSPKSESVTTQAELEEKLTNPVFVGYLCIVLLMLLLLIFWIA
PAHGPTNIMVYISICSLLGSFTVPSTKGIGLAAQDILHNNPSSQRALCLCLVLLAVLGCS
IIVQFRYINKALECFDSSVFGAIYYVVFTTLVLLASAILFREWSNVGLVDFLGMACGFTT
VSVGIVLIQVFKEFNFNLGEMNKSNMKTD
NT seq
990 nt
NT seq
+upstream
nt +downstream
nt
atggggactgcagctgcggcagcggcggcggcggcggcggcggcggccggggagggggcg
cgtagcccgagccccgccgccgtgtcgctcggcctgggcgtggccgtcgtgtcgagcctg
gtgaacgggtccacgttcgtgctacagaagaagggcatcgtgcgtgccaagcggcgaggt
acttcctatttaacagacattgtgtggtgggctggcacaatcgcaatggctgttggccag
attggaaacttcctggcttacacggcggtccccacggtcctggtaacccccctgggcgcc
cttggagtaccgttcgggtccattttagcttcctatctcctgaaggaaaagctcaacatc
ttgggcaagttggggtgcctgctaagctgtgcaggctccgtcgtgctgattatccactcc
ccaaagtctgagagtgtgacaactcaggctgagctggaggaaaagctgaccaatccagtg
tttgtgggctacctgtgcatcgtgctgctcatgctgctgctgctcatcttctggatcgcg
ccggcccatgggcccaccaacatcatggtctacatcagcatctgctccttgctgggcagt
ttcaccgtgccttccaccaagggcatcgggctggcggcccaagacatcttgcataacaac
ccgtccagtcagagagccctctgcctgtgcctggtactcctggccgtgctcggctgcagc
atcatcgtccagttcaggtacatcaacaaggcgctggagtgcttcgactcctcggtgttc
ggggccatctactacgtcgtgtttaccacgctggtcctgctggcctcagccatcctcttc
cgggagtggagcaacgtgggcctggtggacttcttggggatggcctgtggattcacgacc
gtctccgtggggattgtccttatacaggtgttcaaagagttcaatttcaaccttggggag
atgaacaaatctaatatgaaaacagactag
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