KEGG   Homo sapiens (human): 6862
Entry
6862              CDS       T01001                                 
Symbol
TBXT, SAVA, T, TFT
Name
(RefSeq) T-box transcription factor T
  KO
K10172  brachyury protein
Organism
hsa  Homo sapiens (human)
Disease
H02324  Sacral agenesis with vertebral anomalies
H02563  Neural tube defects
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    6862 (TBXT)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Other transcription factors
   T-box
    6862 (TBXT)
SSDB
Motif
Pfam: T-box
Other DBs
NCBI-GeneID: 6862
NCBI-ProteinID: NP_003172
OMIM: 601397
HGNC: 11515
Ensembl: ENSG00000164458
UniProt: O15178
Structure
Position
6:complement(166157656..166168655)
AA seq 435 aa
MSSPGTESAGKSLQYRVDHLLSAVENELQAGSEKGDPTERELRVGLEESELWLRFKELTN
EMIVTKNGRRMFPVLKVNVSGLDPNAMYSFLLDFVAADNHRWKYVNGEWVPGGKPEPQAP
SCVYIHPDSPNFGAHWMKAPVSFSKVKLTNKLNGGGQIMLNSLHKYEPRIHIVRVGGPQR
MITSHCFPETQFIAVTAYQNEEITALKIKYNPFAKAFLDAKERSDHKEMMEEPGDSQQPG
YSQWGWLLPGTSTLCPPANPHPQFGGALSLPSTHSCDRYPTLRSHRSSPYPSPYAHRNNS
PTYSDNSPACLSMLQSHDNWSSLGMPAHPSMLPVSHNASPPTSSSQYPSLWSVSNGAVTP
GSQAAAVSNGLGAQFFRGSPAHYTPLTHPVSAPSSSGSPLYEGAAAATDIVDSQYDAAAQ
GRLIASWTPVSPPSM
NT seq 1308 nt   +upstreamnt  +downstreamnt
atgagctcccctggcaccgagagcgcgggaaagagcctgcagtaccgagtggaccacctg
ctgagcgccgtggagaatgagctgcaggcgggcagcgagaagggcgaccccacagagcgc
gaactgcgcgtgggcctggaggagagcgagctgtggctgcgcttcaaggagctcaccaat
gagatgatcgtgaccaagaacggcaggaggatgtttccggtgctgaaggtgaacgtgtct
ggcctggaccccaacgccatgtactccttcctgctggacttcgtggcggcggacaaccac
cgctggaagtacgtgaacggggaatgggtgccggggggcaagccggagccgcaggcgccc
agctgcgtctacatccaccccgactcgcccaacttcggggcccactggatgaaggctccc
gtctccttcagcaaagtcaagctcaccaacaagctcaacggagggggccagatcatgctg
aactccttgcataagtatgagcctcgaatccacatagtgagagttgggggtccacagcgc
atgatcaccagccactgcttccctgagacccagttcatagcggtgactgcttatcagaac
gaggagatcacagctcttaaaattaagtacaatccatttgcaaaagctttccttgatgca
aaggaaagaagtgatcacaaagagatgatggaggaacccggagacagccagcaacctggg
tactcccaatgggggtggcttcttcctggaaccagcaccctgtgtccacctgcaaatcct
catcctcagtttggaggtgccctctccctcccctccacgcacagctgtgacaggtaccca
accctgaggagccaccggtcctcaccctaccccagcccctatgctcatcggaacaattct
ccaacctattctgacaactcacctgcatgtttatccatgctgcaatcccatgacaattgg
tccagccttggaatgcctgcccatcccagcatgctccccgtgagccacaatgccagccca
cctaccagctccagtcagtaccccagcctgtggtctgtgagcaacggcgccgtcaccccg
ggctcccaggcagcagccgtgtccaacgggctgggggcccagttcttccggggctccccc
gcgcactacacacccctcacccatccggtctcggcgccctcttcctcgggatccccactg
tacgaaggggcggccgcggccacagacatcgtggacagccagtacgacgccgcagcccaa
ggccgcctcatagcctcatggacacctgtgtcgccaccttccatgtga

  All links  
Disease (3)   
   OMIM (3)   
Gene (34)   
   RefGene (20)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (9)   
   OC (1)   
Protein sequence (8)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (6)   
DNA sequence (18)   
   RefSeq(nuc) (6)   
   GenBank (6)   
   EMBL (6)   
3D Structure (56)   
   PDB (56)   
Protein domain (1)   
   Pfam (1)   
All databases (120)   

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