KEGG   Homo sapiens (human): 10120
Entry
10120             CDS       T01001                                 

Gene name
ACTR1B, ARP1B, CTRN2, PC3
Definition
(RefSeq) actin related protein 1B
  KO
K16575  centractin
Organism
hsa  Homo sapiens (human)
Pathway
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05132  Salmonella infection
Network
nt06125  Membrane trafficking (bacteria)
nt06419  Microtubule-based transport
nt06461  Huntington disease
nt06463  Parkinson disease
nt06464  Amyotrophic lateral sclerosis
  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]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    10120 (ACTR1B)
   05016 Huntington disease
    10120 (ACTR1B)
   05022 Pathways of neurodegeneration - multiple diseases
    10120 (ACTR1B)
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    10120 (ACTR1B)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation and ciliogenesis 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)
SSDB
Motif
Pfam: Actin
Other DBs
NCBI-GeneID: 10120
NCBI-ProteinID: NP_005726
OMIM: 605144
HGNC: 168
Ensembl: ENSG00000115073
Vega: OTTHUMG00000130549
Pharos: P42025(Tdark)
UniProt: P42025
LinkDB
Position
2q11.2
AA seq 376 aa
MESYDIIANQPVVIDNGSGVIKAGFAGDQIPKYCFPNYVGRPKHMRVMAGALEGDLFIGP
KAEEHRGLLTIRYPMEHGVVRDWNDMERIWQYVYSKDQLQTFSEEHPVLLTEAPLNPSKN
REKAAEVFFETFNVPALFISMQAVLSLYATGRTTGVVLDSGDGVTHAVPIYEGFAMPHSI
MRVDIAGRDVSRYLRLLLRKEGVDFHTSAEFEVVRTIKERACYLSINPQKDEALETEKVQ
YTLPDGSTLDVGPARFRAPELLFQPDLVGDESEGLHEVVAFAIHKSDMDLRRTLFANIVL
SGGSTLFKGFGDRLLSEVKKLAPKDIKIKISAPQERLYSTWIGGSILASLDTFKKMWVSK
KEYEEDGSRAIHRKTF
NT seq 1131 nt   +upstreamnt  +downstreamnt
atggagtcctacgacatcatcgccaaccagcctgtggtcatcgacaacggttcgggggtg
attaaagctggctttgcaggagaccagattcccaaatactgtttcccaaactatgtcggg
cggccgaagcacatgcgggtgatggctggagccctggagggggacctcttcatcggacca
aaagcagaggagcaccgggggctgctgaccatccgctaccccatggagcacggcgtggtg
cgagactggaacgacatggaacgcatctggcagtacgtctactccaaggatcagctgcag
accttctcggaggagcatcctgtgctcctcacggaggccccgctcaacccgagtaagaac
cgggagaaggcggcagaggtgttctttgagaccttcaacgtgccggccctgttcatctcc
atgcaggctgtgctcagtctgtacgcaacaggacgcacgacaggagtggttctagactca
ggggacggggtcactcatgctgtgcccatctatgagggctttgccatgcctcactccatc
atgcgggtggacattgccggccgcgacgtctcccgctacctccgactcctgctgcgcaag
gaaggggttgacttccatacctcggctgagtttgaggttgtccggacaatcaaagagcga
gcgtgctacctgtccatcaacccacagaaggatgaggctctggagacggagaaggtgcag
tacacgttgccagacggcagcacgcttgatgtggggcctgcacgattccgggcccccgag
ctgctgttccagccggaccttgtcggggatgagagtgaggggctccatgaggtggtggcc
ttcgccatacacaagtccgacatggacctgcgccggacgctgttcgccaacatcgtgctc
tcaggtggctcaacgcttttcaaaggcttcggagaccgattactcagtgaagtgaagaag
cttgccccaaaggatatcaaaatcaagatctcagccccgcaggaacggctgtactccaca
tggattggcggctccatcctggcctcgctggacacttttaagaagatgtgggtgtccaaa
aaggagtatgaagaggatggctcccgtgctattcatcgcaaaactttctag

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