KEGG   Homo sapiens (human): 9760
Entry
9760              CDS       T01001                                 
Symbol
TOX, TOX1
Name
(RefSeq) thymocyte selection associated high mobility group box
Organism
hsa  Homo sapiens (human)
SSDB
Motif
Pfam: HMG_box HMG_box_2 YABBY
Other DBs
NCBI-GeneID: 9760
NCBI-ProteinID: NP_055544
OMIM: 606863
HGNC: 18988
Ensembl: ENSG00000198846
UniProt: O94900
Position
8:complement(58805412..59119147)
AA seq 526 aa
MDVRFYPPPAQPAAAPDAPCLGPSPCLDPYYCNKFDGENMYMSMTEPSQDYVPASQSYPG
PSLESEDFNIPPITPPSLPDHSLVHLNEVESGYHSLCHPMNHNGLLPFHPQNMDLPEITV
SNMLGQDGTLLSNSISVMPDIRNPEGTQYSSHPQMAAMRPRGQPADIRQQPGMMPHGQLT
TINQSQLSAQLGLNMGGSNVPHNSPSPPGSKSATPSPSSSVHEDEGDDTSKINGGEKRPA
SDMGKKPKTPKKKKKKDPNEPQKPVSAYALFFRDTQAAIKGQNPNATFGEVSKIVASMWD
GLGEEQKQVYKKKTEAAKKEYLKQLAAYRASLVSKSYSEPVDVKTSQPPQLINSKPSVFH
GPSQAHSALYLSSHYHQQPGMNPHLTAMHPSLPRNIAPKPNNQMPVTVSIANMAVSPPPP
LQISPPLHQHLNMQQHQPLTMQQPLGNQLPMQVQSALHSPTMQQGFTLQPDYQTIINPTS
TAAQVVTQAMEYVRSGCRNPPPQPVDWNNDYCSSGGMQRDKALYLT
NT seq 1581 nt   +upstreamnt  +downstreamnt
atggacgtaagattttatccacctccagcccagcccgccgctgcgcccgacgctccctgt
ctgggaccttctccctgcctggacccctactattgcaacaagtttgacggtgagaacatg
tatatgagcatgacagagccgagccaggactatgtgccagccagccagtcctaccctggt
ccaagcctggaaagtgaagacttcaacattccaccaattactcctccttccctcccagac
cactcgctggtgcacctgaatgaagttgagtctggttaccattctctgtgtcaccccatg
aaccataatggcctgctaccatttcatccacaaaacatggacctccctgaaatcacagtc
tccaatatgctgggccaggatggaacactgctttctaattccatttctgtgatgccagat
atacgaaacccagaaggaactcagtacagttcccatcctcagatggcagccatgagacca
aggggccagcctgcagacatcaggcagcagccaggaatgatgccacatggccagctgact
accattaaccagtcacagctaagtgctcaacttggtttgaatatgggaggaagcaatgtt
ccccacaactcaccatctccacctggaagcaagtctgcaactccttcaccatccagttca
gtgcatgaagatgaaggcgatgatacctctaagatcaatggtggagagaagcggcctgcc
tctgatatggggaaaaaaccaaaaactcccaaaaagaagaagaagaaggatcccaatgag
ccccagaagcctgtgtctgcctatgcgttattctttcgtgatactcaggccgccatcaag
ggccaaaatccaaacgctacctttggcgaagtctctaaaattgtggcttcaatgtgggac
ggtttaggagaagagcaaaaacaggtctataaaaagaaaaccgaggctgcgaagaaggag
tacctgaagcaactcgcagcatacagagccagccttgtatccaagagctacagtgaacct
gttgacgtgaagacatctcaacctcctcagctgatcaattcgaagccgtcggtgttccat
gggcccagccaggcccactcggccctgtacctaagttcccactatcaccaacaaccggga
atgaatcctcacctaactgccatgcatcctagtctccccaggaacatagcccccaagccg
aataaccaaatgccagtgactgtctctatagcaaacatggctgtgtcccctcctcctccc
ctccagatcagcccgcctcttcaccagcatctcaacatgcagcagcaccagccgctcacc
atgcagcagccccttgggaaccagctccccatgcaggtccagtctgccttacactcaccc
accatgcagcaaggatttactcttcaacccgactatcagactattatcaatcctacatct
acagctgcacaagttgtcacccaggcaatggagtatgtgcgttcggggtgcagaaatcct
cccccacaaccggtggactggaataacgactactgcagtagtgggggcatgcagagggac
aaagcactgtaccttacttga

  All links  
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (12)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
   PHAROS (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (13)   
   RefSeq(nuc) (1)   
   GenBank (6)   
   EMBL (6)   
Protein domain (3)   
   Pfam (3)   
All databases (33)   

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