Homo sapiens (human): 6909 Help Entry 6909              CDS       T01001                                  Symbol TBX2, VETD Name (RefSeq) T-box transcription factor 2   KO K10176   T-box protein 2 Organism hsa  Homo sapiens (human) Disease H02753   Vertebral anomalies and variable endocrine and T-cell dysfunction Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     6909 (TBX2) Transcription factors [BR:hsa03000]  Eukaryotic type   Other transcription factors    T-box     6909 (TBX2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  T-box TBX2-3_RD TBX2-3_TAD Motif Other DBs NCBI-GeneID:  6909 NCBI-ProteinID:  NP_005985 OMIM:  600747 HGNC:  11597 Ensembl:  ENSG00000121068 UniProt:  Q13207 LinkDB All DBs Position 17:61399843..61409466 Genome browser AA seq 712 aa AA seqDB search MREPALAASAMAYHPFHAPRPADFPMSAFLAAAQPSFFPALALPPGALAKPLPDPGLAGA AAAAAAAAAAAEAGLHVSALGPHPPAAHLRSLKSLEPEDEVEDDPKVTLEAKELWDQFHK LGTEMVITKSGRRMFPPFKVRVSGLDKKAKYILLMDIVAADDCRYKFHNSRWMVAGKADP EMPKRMYIHPDSPATGEQWMAKPVAFHKLKLTNNISDKHGFTILNSMHKYQPRFHIVRAN DILKLPYSTFRTYVFPETDFIAVTAYQNDKITQLKIDNNPFAKGFRDTGNGRREKRKQLT LPSLRLYEEHCKPERDGAESDASSCDPPPAREPPTSPGAAPSPLRLHRARAEEKSCAADS DPEPERLSEERAGAPLGRSPAPDSASPTRLTEPERARERRSPERGKEPAESGGDGPFGLR SLEKERAEARRKDEGRKEAAEGKEQGLAPLVVQTDSASPLGAGHLPGLAFSSHLHGQQFF GPLGAGQPLFLHPGQFTMGPGAFSAMGMGHLLASVAGGGNGGGGGPGTAAGLDAGGLGPA ASAASTAAPFPFHLSQHMLASQGIPMPTFGGLFPYPYTYMAAAAAAASALPATSAAAAAA AAAGSLSRSPFLGSARPRLRFSPYQIPVTIPPSTSLLTTGLASEGSKAAGGNSREPSPLP ELALRKVGAPSRGALSPSGSAKEAANELQSIQRLVSGLESQRALSPGRESPK NT seq 2139 nt NT seq  +upstreamnt  +downstreamnt atgagagagccggcgctggcggccagcgccatggcttaccacccgttccacgcgccacgg cccgccgacttccccatgtccgcctttctggcggcggcgcagccctccttcttcccggca ctcgcgctgccgcccggcgcgctggccaagccgctgcccgacccgggcctggcgggggcg gcggccgcggcggcggcggcggcagcagcggccgaggcggggctgcacgtctcggcactg ggcccgcacccgcccgccgcgcatctgcgctccctcaagagcctggagcccgaggacgag gtggaggacgaccccaaggtgacgctggaggccaaggagctgtgggaccagttccacaag ctaggcacggagatggtcatcaccaagtccgggaggcggatgttcccccccttcaaggtg cgagtcagcggcctggacaagaaggccaagtatatcctgctgatggacattgtagccgct gacgattgccgctataagttccacaactcgcgctggatggtggcgggcaaggccgaccct gagatgcccaaacgcatgtacatccacccagacagcccagccacgggggagcagtggatg gctaagcctgtggccttccacaagctgaagctgaccaacaacatctctgacaagcacggc ttcaccatcctaaactccatgcacaagtaccagccgcgcttccacatagtgcgagccaac gacatcctgaagctgccttacagcaccttccgcacctacgtgttcccggagaccgacttc atcgccgtcactgcctaccagaatgacaagatcacacagctgaagatcgacaacaacccg tttgccaagggcttccgggacaccgggaacggccggcgggagaaaaggaagcagctgacg ctgccgtctctacgcttgtacgaggagcactgcaaacccgagcgcgatggcgcggagtca gacgcctcgtcgtgcgaccctccccccgcgcgggaaccacccacctccccgggcgcagcg cccagtccgctgcgcctgcaccgggcccgagctgaggagaagtcgtgcgccgcggacagc gacccggagcctgagcggttgagcgaggagcgtgcgggggcgccgctaggccgcagcccg gctccagacagcgccagccccactcgcttgaccgaacccgagcgcgcccgggagcggcgt agtcccgagaggggcaaggagccggccgagagcggcggggacggcccgttcggcctgagg agcctggagaaggagcgcgccgaagctcggaggaaggacgaggggcgcaaggaggcggcc gagggcaaggagcagggcctggcgccgctggtggtgcagacagacagtgcgtcccccctg ggcgccggacacctgcccggcctggccttttccagccacttgcacgggcagcagttcttt gggccgctgggagccggccagccgctcttcctgcaccctggacagttcaccatgggccct ggcgccttctccgccatgggcatgggtcacctactggcctcggtggcaggcggcggcaac ggcggaggtggcgggcctgggaccgccgcggggctggacgcaggcgggctgggtcccgcg gccagcgcagcaagcaccgccgcgcccttcccgttccacctctcccagcacatgctggca tctcagggaattccaatgcccactttcggaggcctcttcccctacccctacacctacatg gcagcagcagccgcagccgcctcggctttgcccgccactagtgctgcagctgccgccgcc gcagccgccggctccctctcccggagccccttcctgggcagtgcccggccccgactgcgt ttcagcccctatcagatcccggtcaccatcccgcctagcactagcctcctcaccaccggg ctggcctctgagggctccaaggccgctggtggaaacagccgggagcctagccccctgccc gagctggctctccgcaaagtaggggccccatcccgcggtgccctgtcgcccagtggctcg gccaaggaggcggccaatgaactgcagagcatccagagactggtgagtgggctggagagc cagcgagccctctccccaggccgggagtcgcccaagtga

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