KEGG   Homo sapiens (human): 7278
Entry
7278              CDS       T01001                                 

Gene name
TUBA3C, TUBA2, bA408E5.3
Definition
(RefSeq) tubulin alpha 3c
  KO
K07374  tubulin alpha
Organism
hsa  Homo sapiens (human)
Pathway
hsa04145  Phagosome
hsa04210  Apoptosis
hsa04530  Tight junction
hsa04540  Gap junction
hsa05010  Alzheimer disease
hsa05012  Parkinson disease
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05020  Prion disease
hsa05022  Pathways of neurodegeneration - multiple diseases
hsa05130  Pathogenic Escherichia coli infection
hsa05132  Salmonella infection
Network
nt06125  Membrane trafficking (bacteria)
nt06135  Cytoskeletal regulation (viruses and bacteria)
nt06419  Microtubule-based transport
nt06460  Alzheimer disease
nt06461  Huntington disease
nt06463  Parkinson disease
nt06464  Amyotrophic lateral sclerosis
nt06465  Prion disease
  Element
N00976  Retrograde axonal transport
N00977  Mutation-caused aberrant Htt to retrograde axonal transport
N00978  Anterograde axonal transport
N00979  Mutation-caused aberrant Htt to anterograde axonal transport
N01018  Mutation-caused aberrant Abeta to anterograde axonal transport
N01055  Mutation-caused aberrant SNCA to anterograde axonal transport
N01158  Mutation-caused aberrant DCTN1 to retrograde axonal transport
N01285  Microtubule-RHOA signaling pathway
N01286  Escherichia EspG to Microtubule-RHOA signaling pathway
N01295  Rab7-regulated microtubule minus-end directed transport
N01297  Arl8-regulated microtubule plus-end directed transport
N01298  Salmonella SifA to microtubule plus-end directed transport
N01299  Salmonella PipB2 to microtubule plus-end directed transport
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09141 Transport and catabolism
   04145 Phagosome
    7278 (TUBA3C)
  09143 Cell growth and death
   04210 Apoptosis
    7278 (TUBA3C)
  09144 Cellular community - eukaryotes
   04530 Tight junction
    7278 (TUBA3C)
   04540 Gap junction
    7278 (TUBA3C)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    7278 (TUBA3C)
   05012 Parkinson disease
    7278 (TUBA3C)
   05014 Amyotrophic lateral sclerosis
    7278 (TUBA3C)
   05016 Huntington disease
    7278 (TUBA3C)
   05020 Prion disease
    7278 (TUBA3C)
   05022 Pathways of neurodegeneration - multiple diseases
    7278 (TUBA3C)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    7278 (TUBA3C)
   05132 Salmonella infection
    7278 (TUBA3C)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03019 Messenger RNA biogenesis [BR:hsa03019]
    7278 (TUBA3C)
   03036 Chromosome and associated proteins [BR:hsa03036]
    7278 (TUBA3C)
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    7278 (TUBA3C)
   04147 Exosome [BR:hsa04147]
    7278 (TUBA3C)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic type
  mRNA surveillance and transport factors
   mRNA cycle factors
    P-body specific factors
     7278 (TUBA3C)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation and ciliogenesis proteins
   Microtubules and associated factors
    Other tubulins
     7278 (TUBA3C)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Microtubules
   Tubulins
    7278 (TUBA3C)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   7278 (TUBA3C)
  Exosomal proteins of other body fluids (saliva and urine)
   7278 (TUBA3C)
  Exosomal proteins of colorectal cancer cells
   7278 (TUBA3C)
SSDB
Motif
Pfam: Tubulin Tubulin_C Tubulin_3
Other DBs
NCBI-GeneID: 7278
NCBI-ProteinID: NP_005992
OMIM: 602528
HGNC: 12408
Ensembl: ENSG00000198033
Vega: OTTHUMG00000016481
Pharos: Q13748(Tchem)
UniProt: P0DPH7 P0DPH8 Q1ZYQ1
LinkDB
Position
13q12.11
AA seq 450 aa
MRECISIHVGQAGVQIGNACWELYCLEHGIQPDGQMPSDKTIGGGDDSFNTFFSETGAGK
HVPRAVFVDLEPTVVDEVRTGTYRQLFHPEQLITGKEDAANNYARGHYTIGKEIVDLVLD
RIRKLADLCTGLQGFLIFHSFGGGTGSGFASLLMERLSVDYGKKSKLEFAIYPAPQVSTA
VVEPYNSILTTHTTLEHSDCAFMVDNEAIYDICRRNLDIERPTYTNLNRLIGQIVSSITA
SLRFDGALNVDLTEFQTNLVPYPRIHFPLATYAPVISAEKAYHEQLSVAEITNACFEPAN
QMVKCDPRHGKYMACCMLYRGDVVPKDVNAAIATIKTKRTIQFVDWCPTGFKVGINYQPP
TVVPGGDLAKVQRAVCMLSNTTAIAEAWARLDHKFDLMYAKRAFVHWYVGEGMEEGEFSE
AREDLAALEKDYEEVGVDSVEAEAEEGEEY
NT seq 1353 nt   +upstreamnt  +downstreamnt
atgcgtgagtgtatctctatccacgtggggcaggcaggagtccagatcggcaatgcctgc
tgggaactgtactgcctggaacatggaattcagcccgatggtcagatgccaagtgataaa
accattggtggtggggacgactccttcaacacgttcttcagtgagactggagctggcaag
cacgtgcccagagcagtgtttgtggacctggagcccactgtggtcgatgaagtgcgcaca
ggaacctataggcagctcttccacccagagcagctgatcaccgggaaggaagatgcggcc
aataattacgccagaggccattacaccatcggcaaggagatcgtcgacctggtcctggac
cggatccgcaaactggcggatctgtgcacgggactgcagggcttcctcatcttccacagt
tttgggggtggcactggctctgggttcgcatctctgctcatggagcggctctcagtggat
tacggcaagaagtccaagctagaatttgccatttacccagccccccaggtctccacggcc
gtggtggagccctacaactccatcctgaccacccacacgaccctggaacattctgactgt
gccttcatggtcgacaatgaagccatctatgacatatgtcggcgcaacctggacatcgag
cgtcccacgtacaccaacctcaatcgcctgattgggcagatcgtgtcctccatcacggcc
tccctgcgatttgacggggccctgaatgtggacttgacggaattccagaccaacctagtg
ccgtacccccgcatccacttccccctggccacctacgccccggtcatctcagccgagaag
gcctaccacgagcagctgtccgtggctgagatcaccaatgcctgcttcgagccagccaat
cagatggtcaagtgtgaccctcgccacggcaagtacatggcctgctgcatgttgtacagg
ggggatgtggtcccgaaagatgtcaacgcggccatcgccaccatcaagaccaagcgcacc
atccagtttgtagattggtgcccaactggatttaaggtgggcattaactaccagcccccc
acggtggtccctgggggagacctggccaaggtgcagcgggctgtgtgcatgctgagcaac
accacggccatcgcggaggcctgggctcgcctggaccataagttcgatctcatgtatgcc
aagcgggcctttgtgcactggtacgtgggagaaggcatggaggagggggagttctctgag
gcccgcgaggacctggcagctctggagaaggattatgaagaggtgggcgtggattccgtg
gaagccgaggctgaagaaggtgaagaatactga

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