Homo sapiens (human): 10120
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Entry
10120 CDS
T01001
Symbol
ACTR1B, ARP1B, CTRN2, PC3
Name
(RefSeq) actin related protein 1B
KO
K16575
centractin
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
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
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04814 Motor proteins
10120 (ACTR1B)
09160 Human Diseases
09171 Infectious disease: bacterial
05132 Salmonella infection
10120 (ACTR1B)
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
10120 (ACTR1B)
05016 Huntington disease
10120 (ACTR1B)
05022 Pathways of neurodegeneration - multiple diseases
10120 (ACTR1B)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
10120 (ACTR1B)
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
10120 (ACTR1B)
04147 Exosome [BR:
hsa04147
]
10120 (ACTR1B)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Microtubules and associated factors
Dynactin complex
10120 (ACTR1B)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actins
Actin-related proteins
10120 (ACTR1B)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of bladder cancer cells
10120 (ACTR1B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Actin
Motif
Other DBs
NCBI-GeneID:
10120
NCBI-ProteinID:
NP_005726
OMIM:
605144
HGNC:
168
Ensembl:
ENSG00000115073
Pharos:
P42025
(Tdark)
UniProt:
P42025
LinkDB
All DBs
Position
2:complement(97655939..97664044)
Genome browser
AA seq
376 aa
AA seq
DB search
MESYDIIANQPVVIDNGSGVIKAGFAGDQIPKYCFPNYVGRPKHMRVMAGALEGDLFIGP
KAEEHRGLLTIRYPMEHGVVRDWNDMERIWQYVYSKDQLQTFSEEHPVLLTEAPLNPSKN
REKAAEVFFETFNVPALFISMQAVLSLYATGRTTGVVLDSGDGVTHAVPIYEGFAMPHSI
MRVDIAGRDVSRYLRLLLRKEGVDFHTSAEFEVVRTIKERACYLSINPQKDEALETEKVQ
YTLPDGSTLDVGPARFRAPELLFQPDLVGDESEGLHEVVAFAIHKSDMDLRRTLFANIVL
SGGSTLFKGFGDRLLSEVKKLAPKDIKIKISAPQERLYSTWIGGSILASLDTFKKMWVSK
KEYEEDGSRAIHRKTF
NT seq
1131 nt
NT seq
+upstream
nt +downstream
nt
atggagtcctacgacatcatcgccaaccagcctgtggtcatcgacaacggttcgggggtg
attaaagctggctttgcaggagaccagattcccaaatactgtttcccaaactatgtcggg
cggccgaagcacatgcgggtgatggctggagccctggagggggacctcttcatcggacca
aaagcagaggagcaccgggggctgctgaccatccgctaccccatggagcacggcgtggtg
cgagactggaacgacatggaacgcatctggcagtacgtctactccaaggatcagctgcag
accttctcggaggagcatcctgtgctcctcacggaggccccgctcaacccgagtaagaac
cgggagaaggcggcagaggtgttctttgagaccttcaacgtgccggccctgttcatctcc
atgcaggctgtgctcagtctgtacgcaacaggacgcacgacaggagtggttctagactca
ggggacggggtcactcatgctgtgcccatctatgagggctttgccatgcctcactccatc
atgcgggtggacattgccggccgcgacgtctcccgctacctccgactcctgctgcgcaag
gaaggggttgacttccatacctcggctgagtttgaggttgtccggacaatcaaagagcga
gcgtgctacctgtccatcaacccacagaaggatgaggctctggagacggagaaggtgcag
tacacgttgccagacggcagcacgcttgatgtggggcctgcacgattccgggcccccgag
ctgctgttccagccggaccttgtcggggatgagagtgaggggctccatgaggtggtggcc
ttcgccatacacaagtccgacatggacctgcgccggacgctgttcgccaacatcgtgctc
tcaggtggctcaacgcttttcaaaggcttcggagaccgattactcagtgaagtgaagaag
cttgccccaaaggatatcaaaatcaagatctcagccccgcaggaacggctgtactccaca
tggattggcggctccatcctggcctcgctggacacttttaagaagatgtgggtgtccaaa
aaggagtatgaagaggatggctcccgtgctattcatcgcaaaactttctag
DBGET
integrated database retrieval system