Homo sapiens (human): 4869
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Entry
4869 CDS
T01001
Symbol
NPM1, B23, NPM
Name
(RefSeq) nucleophosmin 1
KO
K11276
nucleophosmin 1
Organism
hsa
Homo sapiens (human)
Disease
H00003
Acute myeloid leukemia
H02411
Chronic myelomonocytic leukemia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
4869 (NPM1)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Nucleosome assembly factors
Histone chaperones
Nucleoplasmins
4869 (NPM1)
Centrosome formation proteins
Centrosome duplication proteins
Regulators of centriole replication
4869 (NPM1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Nucleoplasmin
NPM1-C
NPL
YL1
NOA36
Nop14
TFIIF_alpha
CDC45
Motif
Other DBs
NCBI-GeneID:
4869
NCBI-ProteinID:
NP_002511
OMIM:
164040
HGNC:
7910
Ensembl:
ENSG00000181163
UniProt:
P06748
A0A0S2Z491
Structure
PDB
PDBj
LinkDB
All DBs
Position
5:171387116..171410900
Genome browser
AA seq
294 aa
AA seq
DB search
MEDSMDMDMSPLRPQNYLFGCELKADKDYHFKVDNDENEHQLSLRTVSLGAGAKDELHIV
EAEAMNYEGSPIKVTLATLKMSVQPTVSLGGFEITPPVVLRLKCGSGPVHISGQHLVAVE
EDAESEDEEEEDVKLLSISGKRSAPGGGSKVPQKKVKLAADEDDDDDDEEDDDEDDDDDD
FDDEEAEEKAPVKKSIRDTPAKNAQKSNQNGKDSKPSSTPRSKGQESFKKQEKTPKTPKG
PSSVEDIKAKMQASIEKGGSLPKVEAKFINYVKNCFRMTDQEAIQDLWQWRKSL
NT seq
885 nt
NT seq
+upstream
nt +downstream
nt
atggaagattcgatggacatggacatgagccccctgaggccccagaactatcttttcggt
tgtgaactaaaggccgacaaagattatcactttaaggtggataatgatgaaaatgagcac
cagttatctttaagaacggtcagtttaggggctggtgcaaaggatgagttgcacattgtt
gaagcagaggcaatgaattacgaaggcagtccaattaaagtaacactggcaactttgaaa
atgtctgtacagccaacggtttcccttgggggctttgaaataacaccaccagtggtctta
aggttgaagtgtggttcagggccagtgcatattagtggacagcacttagtagctgtggag
gaagatgcagagtcagaagatgaagaggaggaggatgtgaaactcttaagtatatctgga
aagcggtctgcccctggaggtggtagcaaggttccacagaaaaaagtaaaacttgctgct
gatgaagatgatgacgatgatgatgaagaggatgatgatgaagatgatgatgatgatgat
tttgatgatgaggaagctgaagaaaaagcgccagtgaagaaatctatacgagatactcca
gccaaaaatgcacaaaagtcaaatcagaatggaaaagactcaaaaccatcatcaacacca
agatcaaaaggacaagaatccttcaagaaacaggaaaaaactcctaaaacaccaaaagga
cctagttctgtagaagacattaaagcaaaaatgcaagcaagtatagaaaaaggtggttct
cttcccaaagtggaagccaaattcatcaattatgtgaagaattgcttccggatgactgac
caagaggctattcaagatctctggcagtggaggaagtctctttaa
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