Homo sapiens (human): 10528
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Entry
10528 CDS
T01001
Symbol
NOP56, NOL5A, SCA36
Name
(RefSeq) NOP56 ribonucleoprotein
KO
K14564
nucleolar protein 56
Organism
hsa
Homo sapiens (human)
Pathway
hsa03008
Ribosome biogenesis in eukaryotes
hsa05017
Spinocerebellar ataxia
Disease
H00063
Spinocerebellar ataxia (SCA)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09122 Translation
03008 Ribosome biogenesis in eukaryotes
10528 (NOP56)
09160 Human Diseases
09164 Neurodegenerative disease
05017 Spinocerebellar ataxia
10528 (NOP56)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03009 Ribosome biogenesis [BR:
hsa03009
]
10528 (NOP56)
Ribosome biogenesis [BR:
hsa03009
]
Eukaryotic type
Sno RNPs
Box C/D snoRNPs
10528 (NOP56)
Prokaryotic type
10528 (NOP56)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Nop
NOP5NT
Motif
Other DBs
NCBI-GeneID:
10528
NCBI-ProteinID:
NP_006383
OMIM:
614154
HGNC:
15911
Ensembl:
ENSG00000101361
UniProt:
O00567
Structure
PDB
PDBj
LinkDB
All DBs
Position
20:2652632..2658393
Genome browser
AA seq
594 aa
AA seq
DB search
MVLLHVLFEHAVGYALLALKEVEEISLLQPQVEESVLNLGKFHSIVRLVAFCPFASSQVA
LENANAVSEGVVHEDLRLLLETHLPSKKKKVLLGVGDPKIGAAIQEELGYNCQTGGVIAE
ILRGVRLHFHNLVKGLTDLSACKAQLGLGHSYSRAKVKFNVNRVDNMIIQSISLLDQLDK
DINTFSMRVREWYGYHFPELVKIINDNATYCRLAQFIGNRRELNEDKLEKLEELTMDGAK
AKAILDASRSSMGMDISAIDLINIESFSSRVVSLSEYRQSLHTYLRSKMSQVAPSLSALI
GEAVGARLIAHAGSLTNLAKYPASTVQILGAEKALFRALKTRGNTPKYGLIFHSTFIGRA
AAKNKGRISRYLANKCSIASRIDCFSEVPTSVFGEKLREQVEERLSFYETGEIPRKNLDV
MKEAMVQAEEAAAEITRKLEKQEKKRLKKEKKRLAALALASSENSSSTPEECEEMSEKPK
KKKKQKPQEVPQENGMEDPSISFSKPKKKKSFSKEELMSSDLEETAGSTSIPKRKKSTPK
EETVNDPEEAGHRSGSKKKRKFSKEEPVSSGPEEAVGKSSSKKKKKFHKASQED
NT seq
1785 nt
NT seq
+upstream
nt +downstream
nt
atggtgctgttgcacgtgctgtttgagcacgcggtcggctacgcgctgctggcgctgaag
gaagtggaggagatcagtctgctgcagccgcaggtggaggagtctgtgctcaacctgggc
aaattccacagcatcgttcgtctggtggccttttgtccctttgcctcatcccaggttgcc
ttggaaaatgccaacgccgtgtctgaaggggttgttcatgaggacctccgcctgctcttg
gagacccacctgccgtccaaaaagaagaaagtactcttgggagttggggatcccaagatt
ggtgccgcaatacaggaggagttagggtacaactgccagactggaggagtcatagctgag
atcctgcgaggagttcgtctgcacttccacaatctggtgaagggtctgaccgatctgtca
gcttgtaaagcacagctggggctgggacacagctattcccgtgccaaagttaagtttaat
gtgaaccgggtggacaatatgatcatccagtccattagcctcctggaccagctggataag
gacatcaataccttctctatgcgtgtcagggagtggtacgggtatcactttccggagctg
gtgaagatcatcaacgacaatgccacatactgccgtcttgcccagtttattggaaaccga
agggaactgaatgaggacaagctggagaagctggaggagctgacaatggatggggccaag
gctaaggctattctggatgcctcacggtcctccatgggcatggacatatctgccattgac
ttgataaacatcgagagcttctccagtcgtgtggtgtctttatctgaataccgccagagc
ctacacacttacctgcgctccaagatgagccaagtagcccccagcctgtcagccctaatt
ggggaagcggtaggtgcacgtctcatcgcacatgctggcagcctcaccaacctggccaag
tatccagcatccacagtgcagatccttggggctgaaaaggccctgttcagagccctgaag
acaaggggtaacactccaaaatatggactcattttccactccaccttcattggccgagca
gctgccaagaacaaaggccgcatctcccgatacctggcaaacaaatgcagtattgcctca
cgaatcgattgcttctctgaggtgcccacgagtgtattcggggagaagcttcgagaacaa
gttgaagagcgactgtccttctatgagactggagagataccacgaaagaatctggatgtc
atgaaggaagcaatggttcaggcagaggaagcggctgctgagattactaggaagctggag
aaacaggagaagaaacgcttaaagaaggaaaagaaacggctggctgcacttgccctcgcg
tcttcagaaaacagcagtagtactccagaggagtgtgaggagatgagtgaaaaacccaaa
aagaagaaaaagcaaaagccccaggaggttcctcaggagaatggaatggaagacccatct
atctctttctccaaacccaagaaaaagaaatctttttccaaggaggagttgatgagtagc
gatcttgaagagaccgctggcagcaccagtattcccaagaggaagaagtctacacccaag
gaggaaacagttaatgaccctgaggaggcaggccacagaagtggctccaagaaaaagagg
aaattctccaaagaggagccggtcagcagtgggcctgaagaggcggttggcaagagcagc
tccaagaagaagaaaaagttccataaagcatcccaggaagattag
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