KEGG   Homo sapiens (human): 79861Help
Entry
79861             CDS       T01001                                 

Gene name
TUBAL3
Definition
(RefSeq) tubulin alpha like 3
  KO
K07374  
tubulin alpha
Organism
hsa  Homo sapiens (human)
Pathway
Phagosome
Apoptosis
Gap junction
Pathogenic Escherichia coli infection
Brite
KEGG Orthology (KO) [BR:hsa00001]
 Cellular Processes
  Transport and catabolism
   04145 Phagosome
    79861 (TUBAL3)
  Cell growth and death
   04210 Apoptosis
    79861 (TUBAL3)
  Cellular community
   04540 Gap junction
    79861 (TUBAL3)
 Human Diseases
  Infectious diseases
   05130 Pathogenic Escherichia coli infection
    79861 (TUBAL3)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic Type
  mRNA surveillance and transport factors
   mRNA cycle factors
    P-body specific factors
     79861 (TUBAL3)
Chromosome [BR:hsa03036]
 Eukaryotic Type
  Centrosome formation and ciliogenesis proteins
   Microtubules
    Other tubulins
     79861 (TUBAL3)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Microtubules
   Tubulins
    79861 (TUBAL3)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   79861 (TUBAL3)
  Exosomal proteins of other body fluids (saliva and urine)
   79861 (TUBAL3)
  Exosomal proteins of colorectal cancer cells
   79861 (TUBAL3)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif Motif
Other DBs
NCBI-ProteinID: 
NCBI-GeneID: 
HGNC: 
HPRD: 
Ensembl: 
Vega: 
UniProt: 
Position
10p15.1
AA seq 446 aa AA seqDB search
MRECLSIHIGQAGIQIGDACWELYCLEHGIQPNGVVLDTQQDQLENAKMEHTNASFDTFF
CETRAGKHVPRALFVDLEPTVIDGIRTGQHRSLFHPEQLLSGKEDAANNYARGRYSVGSE
VIDLVLERTRKLAEQCGGLQGFLIFRSFGGGTGSGFTSLLMERLTGEYSRKTKLEFSVYP
APRISTAVVEPYNSVLTTHSTTEHTDCTFMVDNEAVYDICHRKLGVECPSHASINRLVVQ
VVSSITASLRFEGPLNVDLIEFQTNLVPYPRIHFPMTAFAPIVSADKAYHEQFSVSDITT
ACFESSNQLVKCDPRLGKYMACCLLYRGDVVPKEVNAAIAATKSRHSVQFVDWCPTGFKV
GINNRPPTVMPGGDLAKVHRSICMLSNTTAIVEAWARLDHKFDLMYAKRAFLHWYLREGM
EEAEFLEAREDLAALERDYEEVAQSF
NT seq 1341 nt NT seq  +upstreamnt  +downstreamnt
atgagggagtgcctttccatccacatcggtcaagctggcatccagattggggacgcctgc
tgggaactctattgcctggaacatggaatccagccaaatggcgttgttcttgacactcaa
caggatcagctggaaaatgcaaaaatggagcacacaaatgcatctttcgataccttcttc
tgtgagacaagagctgggaagcatgtgcctagagcactcttcgtggacttggagccaact
gttatagatgggatccggacgggccagcaccgttcactcttccaccccgagcagctcctt
agcggaaaggaggatgctgctaacaattacgcgcgaggccgttactctgtggggtcggag
gtcatcgaccttgtgctggagaggacccggaagctggcagaacagtgtggtggacttcag
ggatttttgattttccgaagctttggaggaggcactggttcagggtttacgtctctctta
atggagaggctcacaggagaatatagcagaaagactaagctggagttctcggtctaccca
gcccccaggatctccactgctgtggtagagccttataactctgtcctcaccacccactcc
accacagagcacacggactgtaccttcatggtggacaacgaggccgtctatgatatatgc
catcgtaaactcggtgttgaatgcccctctcatgccagcatcaatagattggtggttcag
gtggtatcttccatcactgcctccctccggtttgaagggcccttgaatgtagacctaatt
gaattccagaccaacctggtaccttatccgagaatacatttccccatgacagccttcgcc
cccatcgtctctgctgacaaagcctaccatgagcagttctctgtgtcagacatcaccact
gcctgctttgagtcctccaaccagctggtcaagtgtgatcctcggcttgggaagtacatg
gcctgctgcctactctatagaggggatgtggtccccaaggaagtgaatgcagcaatcgca
gccacgaagtcgaggcactctgttcagtttgtagattggtgtccaactggtttcaaggtg
ggcatcaacaatcggccgcccacggtgatgccgggtggggacctggccaaagtccaccgg
tccatctgcatgctgagcaacaccacggcgattgtggaggcctgggcccgcctggaccac
aagtttgacctcatgtacgccaagagagcatttctgcactggtacctcagagaaggcatg
gaagaagcagagttcttggaggccagggaagatctggcagccctggagagggactatgag
gaagtggcgcaaagtttctga

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