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  
Ontology (2)   
   KEGG BRITE (2)   
Disease (5)   
   KEGG DISEASE (2)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (35)   
   KEGG ORTHOLOGY (1)   
   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 (53)   
   PDB (53)   
Protein domain (1)   
   Pfam (1)   
All databases (123)   

Download RDF
DBGET integrated database retrieval system