Homo sapiens (human): 11258
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Entry
11258 CDS
T01001
Symbol
DCTN3, DCTN-22, DCTN22
Name
(RefSeq) dynactin subunit 3
KO
K10425
dynactin 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa04814
Motor proteins
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05132
Salmonella infection
Network
nt06181
Salmonella
nt06461
Huntington disease
nt06463
Parkinson disease
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06515
Regulation of kinetochore-microtubule interactions
Element
N00976
Retrograde axonal transport
N00977
Mutation-caused aberrant Htt to retrograde axonal transport
N01159
Mutation-caused aberrant TUBA4A to retrograde axonal transport
N01160
Mutation-caused aberrant SOD1 to retrograde axonal transport
N01295
Rab7-regulated microtubule minus-end directed transport
N01534
Dynein recruitment to the kinetochore
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04814 Motor proteins
11258 (DCTN3)
09160 Human Diseases
09171 Infectious disease: bacterial
05132 Salmonella infection
11258 (DCTN3)
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
11258 (DCTN3)
05016 Huntington disease
11258 (DCTN3)
05022 Pathways of neurodegeneration - multiple diseases
11258 (DCTN3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
11258 (DCTN3)
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
11258 (DCTN3)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Microtubules and associated factors
Dynactin complex
11258 (DCTN3)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Microtubules
Tubulin-binding proteins
Dynactins
11258 (DCTN3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Dynactin_p22
DUF4011
Spidroin_MaSp
DivIC
DUF6827
Motif
Other DBs
NCBI-GeneID:
11258
NCBI-ProteinID:
NP_009165
OMIM:
607387
HGNC:
2713
Ensembl:
ENSG00000137100
Pharos:
O75935
(Tdark)
UniProt:
O75935
LinkDB
All DBs
Position
9:complement(34613546..34620495)
Genome browser
AA seq
186 aa
AA seq
DB search
MAGLTDLQRLQARVEELERWVYGPGGARGSRKVADGLVKVQVALGNISSKRERVKILYKK
IEDLIKYLDPEYIDRIAIPDASKLQFILAEEQFILSQVALLEQVNALVPMLDSAHIKAVP
EHAARLQRLAQIHIQQQDQCVEITEESKALLEEYNKTTMLLSKQFVQWDELLCQLEAATQ
VKPAEE
NT seq
561 nt
NT seq
+upstream
nt +downstream
nt
atggcgggtctgactgacttgcagcggctacaggcccgagtggaagagctggagcgctgg
gtgtacgggccgggcggggcgcgcggctcacggaaggtggctgacggcctggtcaaggtg
caggtggctttggggaacatttccagcaagagggagagggtgaagattctctacaaaaag
attgaagatctgatcaagtacctggatcctgagtacatcgaccgcattgccatacctgat
gcctctaagctgcaattcatcctagcagaggagcagtttatcctttcccaggttgcactc
ctggagcaggtgaatgccttggtgcccatgctggacagtgctcacatcaaagccgttcct
gagcatgctgcccgcctgcagcgcttggcccagatccacattcagcagcaggaccagtgt
gtggaaatcactgaggagtccaaggctctcctggaggaatacaacaagactacaatgctt
ctctccaagcaattcgtgcagtgggatgagctactttgccagctagaggccgccacgcaa
gtgaagccagcagaggagtga
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