Capra hircus (goat): 102174773
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Entry
102174773 CDS
T02910
Symbol
PSMD7
Name
(RefSeq) 26S proteasome non-ATPase regulatory subunit 7
KO
K03038
26S proteasome regulatory subunit N8
Organism
chx
Capra hircus (goat)
Pathway
chx03050
Proteasome
chx05010
Alzheimer disease
chx05012
Parkinson disease
chx05014
Amyotrophic lateral sclerosis
chx05016
Huntington disease
chx05017
Spinocerebellar ataxia
chx05020
Prion disease
chx05022
Pathways of neurodegeneration - multiple diseases
chx05169
Epstein-Barr virus infection
Brite
KEGG Orthology (KO) [BR:
chx00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
03050 Proteasome
102174773 (PSMD7)
09160 Human Diseases
09172 Infectious disease: viral
05169 Epstein-Barr virus infection
102174773 (PSMD7)
09164 Neurodegenerative disease
05010 Alzheimer disease
102174773 (PSMD7)
05012 Parkinson disease
102174773 (PSMD7)
05014 Amyotrophic lateral sclerosis
102174773 (PSMD7)
05016 Huntington disease
102174773 (PSMD7)
05017 Spinocerebellar ataxia
102174773 (PSMD7)
05020 Prion disease
102174773 (PSMD7)
05022 Pathways of neurodegeneration - multiple diseases
102174773 (PSMD7)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03051 Proteasome [BR:
chx03051
]
102174773 (PSMD7)
Proteasome [BR:
chx03051
]
Eukaryotic proteasome
Regulatory particles
PA700 (19S proteasome)
non-ATPase subunits
102174773 (PSMD7)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MitMem_reg
JAB
Connexin
Motif
Other DBs
NCBI-GeneID:
102174773
NCBI-ProteinID:
XP_005692253
EnsemblRapid:
ENSCHIG00000031114
UniProt:
A0A452F550
LinkDB
All DBs
Position
18:complement(38246370..38254924)
Genome browser
AA seq
322 aa
AA seq
DB search
MPELAVQKVVVHPLVLLSVVDHFNRIGKVGNQKRVVGVLLGSWQKKVLDVSNSFAVPFDE
DDKDDSVWFLDHDYLENMYGMFKKVNARERIVGWYHTGPKLHKNDIAINELMKRYCPNSV
LVIIDVKPKDLGLPTEAYISVEEVHDDGTPTSKTFEHVTSEIGAEEAEEVGVEHLLRDIK
DTTVGTLSQRITNQVHGLKGLNSKLLDIRGYLEKVATGKLPINHQIIYQLQDVFNLLPDV
SLQEFVKAFYLKTNDQMVVVYLASLIRSVVALHNLINNKIANRDAEKKEGQEKEDSKKDR
KDDKEKEKEKSDVKKEEKKEKK
NT seq
969 nt
NT seq
+upstream
nt +downstream
nt
atgccggagctggcggtgcagaaggtggtggtccaccccctggtgctgctcagtgtggtg
gatcatttcaatcgaataggcaaggttggaaaccaaaaacgtgttgttggtgtgcttttg
gggtcatggcaaaagaaagtactcgatgtatccaacagttttgcagttccttttgatgaa
gacgacaaagatgattctgtctggtttttagaccatgattacttggaaaacatgtatgga
atgtttaagaaggtaaacgccagagaaagaatagttgggtggtaccacacaggccctaaa
ctacacaagaatgacatcgccatcaatgaactcatgaaaagatactgccctaactcagta
ttggtcatcattgatgtgaaaccaaaggacctgggactgcccacagaagcatatatttcg
gtggaagaagttcatgatgatggaactccaacctcaaagacatttgagcacgtaaccagt
gaaattggagcagaggaagctgaggaagtcggagttgaacacttattacgagacatcaaa
gacactacagtgggcactctttcccagcggatcacaaaccaggtccatggtctgaaggga
ctcaactccaagctcctggacatcaggggctacctggagaaggtggccaccggcaagctg
cccatcaaccaccagatcatctaccagctgcaggacgtcttcaacctgctgccagatgtc
agcctgcaggagtttgtcaaggccttttacctgaagaccaacgatcagatggtggtagta
tatttggcctcactgatccgttctgtggttgccttgcacaacctcatcaacaacaagatt
gccaaccgggacgcagaaaagaaagaagggcaagaaaaggaagacagcaaaaaggacaga
aaagatgacaaagagaaagagaaggaaaagagtgatgtaaagaaagaagagaaaaaggag
aaaaaataa
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