Homo sapiens (human): 5250
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Entry
5250 CDS
T01001
Symbol
SLC25A3, OK/SW-cl.48, PHC, PTP, PiC
Name
(RefSeq) solute carrier family 25 member 3
KO
K15102
solute carrier family 25 (mitochondrial phosphate transporter), member 3
Organism
hsa
Homo sapiens (human)
Disease
H01348
Mitochondrial phosphate carrier deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
5250 (SLC25A3)
04147 Exosome [BR:
hsa04147
]
5250 (SLC25A3)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC25: Mitochondrial carrier
5250 (SLC25A3)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of other body fluids (saliva and urine)
5250 (SLC25A3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Mito_carr
Motif
Other DBs
NCBI-GeneID:
5250
NCBI-ProteinID:
NP_005879
OMIM:
600370
HGNC:
10989
Ensembl:
ENSG00000075415
UniProt:
Q00325
A0A024RBH9
Q6MZF9
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All DBs
Position
12:98593686..98606367
Genome browser
AA seq
362 aa
AA seq
DB search
MFSSVAHLARANPFNTPHLQLVHDGLGDLRSSSPGPTGQPRRPRNLAAAAVEEQYSCDYG
SGRFFILCGLGGIISCGTTHTALVPLDLVKCRMQVDPQKYKGIFNGFSVTLKEDGVRGLA
KGWAPTFLGYSMQGLCKFGFYEVFKVLYSNMLGEENTYLWRTSLYLAASASAEFFADIAL
APMEAAKVRIQTQPGYANTLRDAAPKMYKEEGLKAFYKGVAPLWMRQIPYTMMKFACFER
TVEALYKFVVPKPRSECSKPEQLVVTFVAGYIAGVFCAIVSHPADSVVSVLNKEKGSSAS
LVLKRLGFKGVWKGLFARIIMIGTLTALQWFIYDSVKVYFRLPRPPPPEMPESLKKKLGL
TQ
NT seq
1089 nt
NT seq
+upstream
nt +downstream
nt
atgttctcgtccgtggcgcacctggcgcgggcgaaccccttcaacacgccacatctgcag
ctggtgcacgatggtctcggggacctccgcagcagctccccagggcccacgggccagccc
cgccgccctcgcaacctggcagccgccgccgtggaagagcagtatagctgtgactatgga
tctggcagattctttatcctttgtggacttggaggaattattagctgtggcacaacacat
acagcattggttcctctagatctggttaaatgcagaatgcaggtggacccccaaaagtac
aagggcatatttaacggattctcagttacacttaaagaggatggtgttcgtggtttggct
aaaggatgggctccgactttccttggctactccatgcagggactctgcaagtttggcttt
tatgaagtctttaaagtcttgtatagcaatatgcttggagaggagaatacttatctctgg
cgcacatcactatatttggctgcctctgccagtgctgaattctttgctgacattgccctg
gctcctatggaagctgctaaggttcgaattcaaacccagccaggttatgccaacactttg
agggatgcagctcccaaaatgtataaggaagaaggcctaaaagcattctacaagggggtt
gctcctctctggatgagacagataccatacaccatgatgaagttcgcctgctttgaacgt
actgttgaagcactgtacaagtttgtggttcctaagccccgcagtgaatgttcaaagcca
gagcagctggttgtaacatttgtagcaggttacatagctggagtcttttgtgcaattgtt
tctcaccctgctgattctgtggtatctgtgttgaataaagaaaaaggtagcagtgcttct
ctggtcctcaagagacttggatttaaaggtgtatggaagggactgtttgcccgtatcatc
atgattggtaccctgactgcactacagtggtttatctatgactccgtgaaggtctacttc
agacttcctcgccctcctccacccgagatgccagagtctctgaagaagaagcttgggtta
actcagtag
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