Homo sapiens (human): 84790 Entry 84790             CDS       T01001                                  Gene name TUBA1C, TUBA6, bcm948 Definition (RefSeq) tubulin alpha 1c   KO K07374   tubulin alpha Organism hsa  Homo sapiens (human) Pathway hsa04145   Phagosome hsa04210   Apoptosis hsa04530   Tight junction hsa04540   Gap junction hsa05130   Pathogenic Escherichia coli infection Brite KEGG Orthology (KO) [BR:hsa00001]  Cellular Processes   Transport and catabolism    04145 Phagosome     84790 (TUBA1C)   Cell growth and death    04210 Apoptosis     84790 (TUBA1C)   Cellular community - eukaryotes    04530 Tight junction     84790 (TUBA1C)    04540 Gap junction     84790 (TUBA1C)  Human Diseases   Infectious diseases    05130 Pathogenic Escherichia coli infection     84790 (TUBA1C) Messenger RNA biogenesis [BR:hsa03019]  Eukaryotic Type   mRNA surveillance and transport factors    mRNA cycle factors     P-body specific factors      84790 (TUBA1C) Chromosome and associated proteins [BR:hsa03036]  Eukaryotic Type   Centrosome formation and ciliogenesis proteins    Microtubules and associated factors     Other tubulins      84790 (TUBA1C) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Microtubules    Tubulins     84790 (TUBA1C) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)    84790 (TUBA1C)   Exosomal proteins of other body fluids (saliva and urine)    84790 (TUBA1C)   Exosomal proteins of colorectal cancer cells    84790 (TUBA1C) SSDB Motif Pfam:  Tubulin Tubulin_C Tubulin_3 Other DBs NCBI-GeneID:  84790 NCBI-ProteinID:  NP_116093 HGNC:  20768 Ensembl:  ENSG00000167553 Vega:  OTTHUMG00000169497 Pharos:  Q9BQE3(Tchem) UniProt:  Q9BQE3 LinkDB Position 12q13.12 AA seq 449 aa MRECISIHVGQAGVQIGNACWELYCLEHGIQPDGQMPSDKTIGGGDDSFNTFFSETGAGK HVPRAVFVDLEPTVIDEVRTGTYRQLFHPEQLITGKEDAANNYARGHYTIGKEIIDLVLD RIRKLADQCTGLQGFLVFHSFGGGTGSGFTSLLMERLSVDYGKKSKLEFSIYPAPQVSTA VVEPYNSILTTHTTLEHSDCAFMVDNEAIYDICRRNLDIERPTYTNLNRLISQIVSSITA SLRFDGALNVDLTEFQTNLVPYPRIHFPLATYAPVISAEKAYHEQLTVAEITNACFEPAN QMVKCDPRHGKYMACCLLYRGDVVPKDVNAAIATIKTKRTIQFVDWCPTGFKVGINYQPP TVVPGGDLAKVQRAVCMLSNTTAVAEAWARLDHKFDLMYAKRAFVHWYVGEGMEEGEFSE AREDMAALEKDYEEVGADSADGEDEGEEY NT seq 1350 nt   +upstreamnt  +downstreamnt atgcgtgagtgcatctccatccacgttggccaggctggtgtccagattggcaatgcctgc tgggagctctactgcctggaacacggcatccagcccgatggccagatgccaagtgacaag accattgggggaggagatgattccttcaacaccttcttcagtgaaacgggtgctggcaag catgtgccccgggcagtgtttgtagacttggaacccacagtcattgatgaagttcgcact ggcacttaccgccagctcttccaccctgagcaactcatcacaggcaaggaagatgctgcc aataactatgcccgagggcactacaccattggcaaggagatcattgacctcgtgttggac cgaattcgcaagctggctgaccagtgcaccggtcttcagggcttcttggttttccacagc tttggtgggggaactggttctgggttcacctcgctgctcatggaacgtctctcagttgat tatggcaagaagtccaagctggagttctccatttacccggcgccccaggtttccacagct gtagttgagccctacaactccatcctcaccacccacaccaccctggagcactctgattgt gccttcatggtagacaatgaggccatctatgacatctgtcgtagaaacctcgatatcgag cgcccaacctacactaaccttaaccgccttattagccagattgtgtcctccatcactgct tccctgagatttgatggagccctgaatgttgacctgacagaattccagaccaacctggtg ccctacccccgcatccacttccctctggccacatatgcccctgtcatctctgctgagaaa gcctaccacgaacagcttactgtagcagagatcaccaatgcttgctttgagccagccaac cagatggtgaaatgtgaccctcgccatggtaaatacatggcttgctgcctgttataccgt ggtgacgtggttcccaaagatgtcaatgctgccattgccaccatcaaaaccaagcgtacc atccagtttgtggattggtgccccactggcttcaaggttggcattaattaccagcctccc actgtggtgcctggcggagacctggccaaggtacagagagctgtgtgcatgctgagcaat accacagctgttgccgaggcctgggctcgcctggaccacaagtttgacctgatgtatgcc aagcgtgcctttgttcactggtacgtgggtgaggggatggaggaaggcgagttttcagag gcccgtgaggacatggctgcccttgagaaggattatgaggaggttggagcagatagtgct gacggagaggatgagggtgaagagtattaa

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