Homo sapiens (human): 115286
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Entry
115286 CDS
T01001
Symbol
SLC25A26, COXPD28, SAMC
Name
(RefSeq) solute carrier family 25 member 26
KO
K15111
solute carrier family 25 (mitochondrial S-adenosylmethionine transporter), member 26
Organism
hsa
Homo sapiens (human)
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
115286 (SLC25A26)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC25: Mitochondrial carrier
115286 (SLC25A26)
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Ortholog
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Gene cluster
GFIT
Motif
Pfam:
Mito_carr
Motif
Other DBs
NCBI-GeneID:
115286
NCBI-ProteinID:
NP_775742
OMIM:
611037
HGNC:
20661
Ensembl:
ENSG00000144741
UniProt:
Q70HW3
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Position
3:66133610..66378927
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AA seq
274 aa
AA seq
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MDRPGFVAALVAGGVAGVSVDLILFPLDTIKTRLQSPQGFSKAGGFHGIYAGVPSAAIGS
FPNAAAFFITYEYVKWFLHADSSSYLTPMKHMLAASAGEVVACLIRVPSEVVKQRAQVSA
STRTFQIFSNILYEEGIQGLYRGYKSTVLREIPFSLVQFPLWESLKALWSWRQDHVVDSW
QSAVCGAFAGGFAAAVTTPLDVAKTRITLAKAGSSTADGNVLSVLHGVWRSQGLAGLFAG
VFPRMAAISLGGFIFLGAYDRTHSLLLEVGRKSP
NT seq
825 nt
NT seq
+upstream
nt +downstream
nt
atggaccggccggggttcgtggcagcgctggtggctggtggggtagcaggtgtttctgtt
gacttgatattatttcctctggataccattaaaaccaggctgcagagtccccaaggattt
agtaaggctggtggttttcatggaatatatgctggcgttccttctgctgctattggatcc
tttcctaatgctgctgcattttttatcacctatgaatatgtgaagtggtttttgcatgct
gattcatcttcatatttgacacctatgaaacatatgttggctgcctctgctggagaagtg
gttgcctgcctgattcgagttccatctgaagtggttaagcagagggcacaggtatctgct
tctacaagaacatttcagattttctctaacatcttatatgaagagggtatccaagggttg
tatcgaggctataaaagcacagttttaagagagattcctttttctttggtccagtttccc
ttatgggagtccttaaaagccctctggtcctggaggcaggatcatgtggtggattcttgg
cagtcagcagtctgtggagcttttgcaggtggatttgccgctgcagtcaccacccctcta
gacgtggcaaagacaagaattacgctggcaaaggctggctccagcactgctgatgggaat
gtgctctctgtcctgcatggggtctggcggtcacaggggctggcaggattatttgcaggt
gtcttccctcgaatggcagccatcagtctgggaggtttcatctttctgggggcttatgac
cgaacgcacagcttgctgttggaagttggcagaaagagtccttga
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