Homo sapiens (human): 84833
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Entry
84833 CDS
T01001
Symbol
ATP5MK, AGP, ATP5MD, DAPIT, HCVFTP2, MC5DN6, USMG5, bA792D24.4
Name
(RefSeq) ATP synthase F(0) complex subunit k, mitochondrial
KO
K18194
up-regulated during skeletal muscle growth protein 5
Organism
hsa
Homo sapiens (human)
Disease
H01369
ATP synthase deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
84833 (ATP5MK)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitochondrial respiratory chain complex assembly factors
Complex-V assembly factors
84833 (ATP5MK)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
ATP_synth_reg
Motif
Other DBs
NCBI-GeneID:
84833
NCBI-ProteinID:
NP_001193355
OMIM:
615204
HGNC:
30889
UniProt:
Q96IX5
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All DBs
Position
10:complement(103389050..103396475)
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AA seq
58 aa
AA seq
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MAGPESDAQYQFTGIKKYFNSYTLTGRMNCVLATYGSIALIVLYFKLRSKKTPAVKAT
NT seq
177 nt
NT seq
+upstream
nt +downstream
nt
atggcaggtccagaaagtgatgcgcaataccagttcactggtattaaaaaatatttcaac
tcttatactctcacaggtagaatgaactgtgtactggccacatatggaagcattgcattg
attgtcttatatttcaagttaaggtccaaaaaaactccagctgtgaaagcaacataa
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