Homo sapiens (human): 10478
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Entry
10478 CDS
T01001
Symbol
SLC25A17, PMP34
Name
(RefSeq) solute carrier family 25 member 17
KO
K13354
solute carrier family 25 (peroxisomal adenine nucleotide transporter), member 17
Organism
hsa
Homo sapiens (human)
Pathway
hsa04146
Peroxisome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04146 Peroxisome
10478 (SLC25A17)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
10478 (SLC25A17)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC25: Mitochondrial carrier
10478 (SLC25A17)
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Ortholog
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Gene cluster
GFIT
Motif
Pfam:
Mito_carr
Motif
Other DBs
NCBI-GeneID:
10478
NCBI-ProteinID:
NP_006349
OMIM:
606795
HGNC:
10987
Ensembl:
ENSG00000100372
Pharos:
O43808
(Tbio)
UniProt:
O43808
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Position
22:complement(40769630..40819346)
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AA seq
307 aa
AA seq
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MASVLSYESLVHAVAGAVGSVTAMTVFFPLDTARLRLQVDEKRKSKTTHMVLLEIIKEEG
LLAPYRGWFPVISSLCCSNFVYFYTFNSLKALWVKGQHSTTGKDLVVGFVAGVVNVLLTT
PLWVVNTRLKLQGAKFRNEDIVPTNYKGIIDAFHQIIRDEGISALWNGTFPSLLLVFNPA
IQFMFYEGLKRQLLKKRMKLSSLDVFIIGAVAKAIATTVTYPLQTVQSILRFGRHRLNPE
NRTLGSLRNILYLLHQRVRRFGIMGLYKGLEAKLLQTVLTAALMFLVYEKLTAATFTVMG
LKRAHQH
NT seq
924 nt
NT seq
+upstream
nt +downstream
nt
atggcttccgtgctgtcctacgaaagcctggtccacgccgtggccggagccgtgggaagc
gtgacagcaatgacagtgttttttcccctggatacagctagacttcgacttcaggttgat
gagaaaagaaaatccaaaactacacacatggtgctcctggagatcattaaagaagaagga
ctcctggcaccatatcgagggtggtttccagtgatttccagtctctgctgctccaatttt
gtctatttctacacttttaatagcctcaaagcactctgggtcaaaggtcaacattctacc
actggaaaagatctggtagttgggtttgttgcaggagtggttaatgtgttgctaacaact
ccactctgggtggtaaacaccagactgaagcttcaaggagcaaaatttaggaatgaagac
attgtaccaacaaactacaaaggtatcattgatgcttttcatcagatcattcgcgatgaa
ggaatctcggctttatggaatggcacatttccctcattgctgttggtcttcaatcctgcc
atccagttcatgttttatgaaggtttaaaacggcagcttttaaagaaacggatgaagctt
tcttccttggatgtgttcatcattggtgcagtagccaaagcgattgccaccacggtgacc
tatcccctgcagacggtacagtcaattctgaggtttgggcgtcatagactaaacccagaa
aacagaacattgggaagtcttcggaatattctctatcttcttcaccaacgagtaagacgt
tttggaataatgggactctacaaaggccttgaagccaaactgctgcagacagtcctcact
gctgctctcatgttccttgtttatgagaaactgacagctgccaccttcacagttatgggg
ctgaagcgtgcacaccaacactga
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