Homo sapiens (human): 51002
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Entry
51002 CDS
T01001
Symbol
TPRKB, CGI-121, CGI121, GAMOS5
Name
(RefSeq) TP53RK binding protein
KO
K15901
EKC/KEOPS complex subunit TPRKB/CGI121
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
]
51002 (TPRKB)
Transfer RNA biogenesis [BR:
hsa03016
]
Eukaryotic type
tRNA modification factors
KEOPS/EKC complex
51002 (TPRKB)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CGI-121
Staph_reg_Sar_Rot
Motif
Other DBs
NCBI-GeneID:
51002
NCBI-ProteinID:
NP_001317317
OMIM:
608680
HGNC:
24259
Ensembl:
ENSG00000144034
UniProt:
Q9Y3C4
Structure
PDB
LinkDB
All DBs
Position
2:complement(73729873..73737345)
Genome browser
AA seq
175 aa
AA seq
DB search
MQLTHQLDLFPECRVTLLLFKDVKNAGDLRRKAMEGTIDGSLINPTVIVDPFQILVAANK
AVHLYKLGKMKTRTLSTEIIFNLSPNNNISEALKKFGISANDTSILIVYIEEGEKQINQE
YLISQVEGHQVSLKNLPEIMNITEVKKIYKLSSQEESIGTLLDAIICRMSTKDVL
NT seq
528 nt
NT seq
+upstream
nt +downstream
nt
atgcagttaacacatcagctggacctatttcccgaatgcagggtaacccttctgttattt
aaagatgtaaaaaatgcgggagacttgagaagaaaggccatggaaggcaccatcgatgga
tcactgataaatcctacagtgattgttgatccatttcagatacttgtggcagcaaacaaa
gcagttcacctctacaaactgggaaaaatgaagacaagaactctatctactgaaattatt
ttcaacctttccccaaataacaatatttcagaggctttgaaaaaatttggtatctcagca
aatgacacttcaattctaattgtttacattgaagagggagaaaaacaaataaatcaagaa
tacctaatatctcaagtagaaggtcatcaggtttctctgaaaaatcttcctgaaataatg
aatattacagaagtcaaaaagatatataaactctcttcacaagaagaaagtattgggaca
ttattggatgctatcatttgtagaatgtcaacaaaagatgttttatga
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integrated database retrieval system
