Homo sapiens (human): 55860
Help
Entry
55860 CDS
T01001
Symbol
ACTR10, ACTR11, Arp10, Arp11, HARP11
Name
(RefSeq) actin related protein 10
KO
K16576
actin-related protein 10
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
55860 (ACTR10)
09160 Human Diseases
09171 Infectious disease: bacterial
05132 Salmonella infection
55860 (ACTR10)
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
55860 (ACTR10)
05016 Huntington disease
55860 (ACTR10)
05022 Pathways of neurodegeneration - multiple diseases
55860 (ACTR10)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
55860 (ACTR10)
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
55860 (ACTR10)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Microtubules and associated factors
Dynactin complex
55860 (ACTR10)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actins
Actin-related proteins
55860 (ACTR10)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Actin
Motif
Other DBs
NCBI-GeneID:
55860
NCBI-ProteinID:
NP_060947
OMIM:
619731
HGNC:
17372
Ensembl:
ENSG00000131966
Pharos:
Q9NZ32
(Tdark)
UniProt:
Q9NZ32
LinkDB
All DBs
Position
14:58200149..58235636
Genome browser
AA seq
417 aa
AA seq
DB search
MPLYEGLGSGGEKTAVVIDLGEAFTKCGFAGETGPRCIIPSVIKRAGMPKPVRVVQYNIN
TEELYSYLKEFIHILYFRHLLVNPRDRRVVIIESVLCPSHFRETLTRVLFKYFEVPSVLL
APSHLMALLTLGINSAMVLDCGYRESLVLPIYEGIPVLNCWGALPLGGKALHKELETQLL
EQCTVDTSVAKEQSLPSVMGSVPEGVLEDIKARTCFVSDLKRGLKIQAAKFNIDGNNERP
SPPPNVDYPLDGEKILHILGSIRDSVVEILFEQDNEEQSVATLILDSLIQCPIDTRKQLA
ENLVVIGGTSMLPGFLHRLLAEIRYLVEKPKYKKALGTKTFRIHTPPAKANCVAWLGGAI
FGALQDILGSRSVSKEYYNQTGRIPDWCSLNNPPLEMMFDVGKTQPPLMKRAFSTEK
NT seq
1254 nt
NT seq
+upstream
nt +downstream
nt
atgccgctctacgagggcctggggagcggcggggagaagacggcggtcgtgatcgacctg
ggagaggcctttaccaagtgtggatttgctggagaaactggtccaagatgtataattcct
agtgtgataaaaagagctgggatgcctaagcctgtcagagttgttcagtataatatcaat
acagaagaattatattcctacctaaaggaattcatccacatactatatttcaggcatcta
ttggtgaatcccagagaccgccgagttgtgattatcgaatcggtattatgtccttctcac
ttcagagagacactcactcgtgttcttttcaaatattttgaggttccatctgtcttgctt
gctccaagtcatctaatggctcttctgacgcttggaattaattctgccatggtcctagat
tgtggatatagggaaagcctggtgttacccatatatgaaggaatcccagttctaaattgt
tggggagcactacccctaggaggaaaagctcttcacaaagagttggaaactcaactattg
gaacaatgtactgttgacacaagtgttgctaaagaacagagccttccctcagtgatgggt
tcagttccggaaggtgtcttagaggacattaaagcgcgtacttgctttgtaagtgatctg
aagcgaggactaaaaatccaagcagcaaaatttaatattgatgggaataatgagcgtccc
tccccacccccaaatgttgactatccattagatggagagaagattttacatatccttgga
tcaatcagagattcagttgtggaaattctttttgaacaagataatgaagagcaatcagtt
gccactttaatattggattcccttatacagtgtccgatagacaccaggaagcaactagca
gagaatttggtagtcataggtggcacttctatgttgccaggatttctccacagattgctt
gcagaaataaggtatttggtagaaaaaccaaaatataaaaaagcacttggcactaagaca
tttcgaattcatactccacctgcaaaagctaattgtgtggcctggttgggaggggctatt
tttggagcattacaagatatacttgggagccgttctgtttcaaaggaatattataatcag
acgggccgtatacctgattggtgttctctcaataacccacctttggaaatgatgtttgat
gtcgggaaaactcaaccacctctgatgaagagagcattttccactgagaaatag
DBGET
integrated database retrieval system
