Homo sapiens (human): 5715
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Entry
5715 CDS
T01001
Symbol
PSMD9, Rpn4, p27
Name
(RefSeq) proteasome 26S subunit, non-ATPase 9
KO
K06693
26S proteasome regulatory subunit N4
Organism
hsa
Homo sapiens (human)
Pathway
hsa03050
Proteasome
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05017
Spinocerebellar ataxia
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
Network
nt06460
Alzheimer disease
nt06461
Huntington disease
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06465
Prion disease
nt06466
Pathways of neurodegeneration
Element
N01029
26S proteasome-mediated protein degradation
N01030
Mutation-caused aberrant SNCA to 26S proteasome-mediated protein degradation
N01060
Mutation-caused aberrant Abeta to 26S proteasome-mediated protein degradation
N01061
Mutation-caused aberrant Htt to 26S proteasome-mediated protein degradation
N01144
Mutation-caused aberrant SOD1 to 26S proteasome-mediated protein degradation
N01145
Mutation-inactivated VCP to 26S proteasome-mediated protein degradation
N01146
Mutation-inactivated UBQLN2 to 26S proteasome-mediated protein degradation
N01197
Scrapie conformation PrPSc to 26S proteasome-mediated protein degradation
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
5715 (PSMD9)
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
5715 (PSMD9)
05012 Parkinson disease
5715 (PSMD9)
05014 Amyotrophic lateral sclerosis
5715 (PSMD9)
05016 Huntington disease
5715 (PSMD9)
05017 Spinocerebellar ataxia
5715 (PSMD9)
05020 Prion disease
5715 (PSMD9)
05022 Pathways of neurodegeneration - multiple diseases
5715 (PSMD9)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
hsa03051
]
5715 (PSMD9)
Proteasome [BR:
hsa03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
non-ATPase subunits
5715 (PSMD9)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Nas2_N
PDZ_6
PDZ_2
PDZ
GRASP55_65
Motif
Other DBs
NCBI-GeneID:
5715
NCBI-ProteinID:
NP_002804
OMIM:
603146
HGNC:
9567
Ensembl:
ENSG00000110801
UniProt:
O00233
LinkDB
All DBs
Position
12:121888790..121918297
Genome browser
AA seq
223 aa
AA seq
DB search
MSDEEARQSGGSSQAGVVTVSDVQELMRRKEEIEAQIKANYDVLESQKGIGMNEPLVDCE
GYPRSDVDLYQVRTARHNIICLQNDHKAVMKQVEEALHQLHARDKEKQARDMAEAHKEAM
SRKLGQSESQGPPRAFAKVNSISPGSPASIAGLQVDDEIVEFGSVNTQNFQSLHNIGSVV
QHSEGKPLNVTVIRRGEKHQLRLVPTRWAGKGLLGCNIIPLQR
NT seq
672 nt
NT seq
+upstream
nt +downstream
nt
atgtccgacgaggaagcgaggcagagcggaggctcctcgcaggccggcgtcgtgactgtc
agcgacgtccaggagctgatgcggcgcaaggaggagatagaagcgcagatcaaggccaac
tatgacgtgctggaaagccaaaaaggcattgggatgaacgagccgctggtggactgtgag
ggctacccccggtcagacgtggacctgtaccaagtccgcaccgccaggcacaacatcata
tgcctgcagaatgatcacaaggcagtgatgaagcaggtggaggaggccctgcaccagctg
cacgctcgcgacaaggagaagcaggcccgggacatggctgaggcccacaaagaggccatg
agccgcaaactgggtcagagtgagagccagggccctccacgggccttcgccaaagtgaac
agcatcagccccggctccccagccagcatcgcgggtctgcaagtggatgatgagattgtg
gagttcggctctgtgaacacccagaacttccagtcactgcataacattggcagtgtggtg
cagcacagtgaggggaagcccctgaatgtgacagtgatccgcaggggggaaaaacaccag
cttagacttgttccaacacgctgggcaggaaaaggactgctgggctgcaacattattcct
ctgcaaagatga
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integrated database retrieval system