Homo sapiens (human): 84520
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Entry
84520 CDS
T01001
Symbol
GON7, C14orf142, PNAS-127
Name
(RefSeq) GON7 subunit of KEOPS complex
KO
K15903
EKC/KEOPS complex subunit GON7
Organism
hsa
Homo sapiens (human)
Disease
H01722
Galloway-Mowat syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03016 Transfer RNA biogenesis [BR:
hsa03016
]
84520 (GON7)
Transfer RNA biogenesis [BR:
hsa03016
]
Eukaryotic type
tRNA modification factors
KEOPS/EKC complex
84520 (GON7)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DUF4611
Motif
Other DBs
NCBI-GeneID:
84520
NCBI-ProteinID:
NP_115879
OMIM:
617436
HGNC:
20356
Ensembl:
ENSG00000170270
UniProt:
Q9BXV9
Structure
PDB
LinkDB
All DBs
Position
14:complement(93202894..93207065)
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AA seq
100 aa
AA seq
DB search
MELLGEYVGQEGKPQKLRVSCEAPGDGDPFQGLLSGVAQMKDMVTELFDPLVQGEVQHRV
AAAPDEDLDGDDEDDAEDENNIDNRTNFDGPSAKRPKTPS
NT seq
303 nt
NT seq
+upstream
nt +downstream
nt
atggagctgctgggagagtacgtcgggcaggaagggaagccgcagaagctgcgggtgtcc
tgtgaggcgccgggtgacggcgaccctttccagggcctgttgtctggcgtggcccagatg
aaggacatggtaacggaattattcgaccctctggtacagggggaagtgcagcaccgggtg
gcggcggctccagacgaggacttggacggtgatgatgaagatgatgcagaagatgaaaat
aacattgataacagaactaacttcgatggaccatctgcaaaacggccaaaaacaccgtct
taa
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