Neogale vison (American mink): 122906065
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Entry
122906065 CDS
T08764
Symbol
PSMD12
Name
(RefSeq) 26S proteasome non-ATPase regulatory subunit 12
KO
K03035
26S proteasome regulatory subunit N5
Organism
nvs
Neogale vison (American mink)
Pathway
nvs03050
Proteasome
nvs05010
Alzheimer disease
nvs05012
Parkinson disease
nvs05014
Amyotrophic lateral sclerosis
nvs05016
Huntington disease
nvs05017
Spinocerebellar ataxia
nvs05020
Prion disease
nvs05022
Pathways of neurodegeneration - multiple diseases
nvs05169
Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
122906065 (PSMD12)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
122906065 (PSMD12)
09164 Neurodegenerative disease
05010 Alzheimer disease
122906065 (PSMD12)
05012 Parkinson disease
122906065 (PSMD12)
05014 Amyotrophic lateral sclerosis
122906065 (PSMD12)
05016 Huntington disease
122906065 (PSMD12)
05017 Spinocerebellar ataxia
122906065 (PSMD12)
05020 Prion disease
122906065 (PSMD12)
05022 Pathways of neurodegeneration - multiple diseases
122906065 (PSMD12)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
nvs03051
]
122906065 (PSMD12)
Proteasome [BR:
nvs03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
non-ATPase subunits
122906065 (PSMD12)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PSMD12-CSN4_N
PCI
RPN5_C
Motif
Other DBs
NCBI-GeneID:
122906065
NCBI-ProteinID:
XP_044103529
LinkDB
All DBs
Position
5:complement(13452218..13481158)
Genome browser
AA seq
474 aa
AA seq
DB search
MTSGGRSRGTSRDVQAGTMADGGSERADGRIVKMEVDYSATVDQRLPECEKLAKEGRLQE
VIETLLSLEKQTRTASDMVSTSRILVAVVKMCYEAKEWDLLNENIMLLSKRRSQLKQAVA
KMVQQCCTYVEEITDLPIKLRLIDTLRMVTEGKIYVEIERARLTKTLATIKEQNGDVKEA
ASILQELQVETYGSMEKKERVEFILEQMRLCLAVKDYIRTQIISKKINTKFFQEENTEKL
KLKYYNLMIQLDQHEGSYLSICKHYRAIYDTPCIQAESEKWQQALKSVVLYVILAPFDNE
QSDLVHRISGDKKLEEIPKYKDLLKLFTTMELMRWSTLVEDYGMELRKGSLESPATDVFG
STEEGERRWKDLKNRVVEHNIRIMAKYYTRITMKRMAQLLDLSVDESEAFLSNLVVNKTI
FAKVDRLAGIINFQRPKDPNNLLNDWSQKLNSLMSLVNKTTHLIAKEEMIHNLQ
NT seq
1425 nt
NT seq
+upstream
nt +downstream
nt
atgacgagtggtggccgaagcagggggacatctagggacgttcaggcagggaccatggcg
gacggcggctcggagcgggctgatgggcgcatcgtcaagatggaggtggactacagcgcc
acggtggatcagcgactgccggagtgcgagaagctggccaaggaaggaagacttcaagaa
gtcattgaaacccttctctctttggagaaacagacccgcactgcttctgatatggtgtct
acatcccgcatcttagttgcggtagtgaagatgtgctatgaggctaaagaatgggattta
cttaatgaaaatattatgcttttgtcaaaaagacggagtcagttaaaacaagctgttgca
aaaatggttcagcagtgttgtacttatgttgaggaaatcacagaccttccaatcaaactt
cgattaattgatactctacgaatggttacagaagggaagatttatgttgaaattgagcgt
gctcggctgacaaaaacattagcaactataaaagaacaaaacggtgatgtgaaggaggca
gcctccattttacaggagttacaggtggaaacctacgggtcaatggaaaagaaggagaga
gtggagtttattttggagcaaatgaggctctgcctagctgtgaaggattacattcgcaca
caaatcatcagcaagaaaattaacaccaaatttttccaggaagaaaatacagagaaatta
aagttgaaatattataatttaatgattcagctggatcagcatgaggggtcctatttgtct
atttgtaagcactacagagcaatatatgatactccttgtatacaggccgaaagcgaaaag
tggcaacaggctctgaaaagtgttgtcctctatgtgatcttggctccttttgacaacgaa
cagtcagatttggttcaccgaataagtggtgacaagaagttagaagaaatccctaaatac
aaggatcttttaaaactttttaccacaatggagctgatgcgttggtccacacttgttgaa
gactacggaatggaattaagaaaaggatctcttgagagtccggcaactgatgtttttggt
tctacagaggaaggtgaaagaaggtggaaagacttgaagaacagagttgttgaacataat
attagaataatggccaagtattacacaaggataacaatgaagagaatggctcagcttctt
gatctgtctgttgatgagtcagaagcttttctttcgaatctagtagttaacaagaccatc
tttgctaaagtagacaggttggcaggaattatcaacttccagagacccaaggatccaaat
aatttattaaatgactggtctcagaaactgaactcactgatgtctctagttaacaaaact
acacacctcatagccaaagaggagatgatacataatctacaataa
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