Homo sapiens (human): 6887 Help Entry 6887              CDS       T01001                                  Symbol TAL2 Name (RefSeq) TAL bHLH transcription factor 2   KO K09068   T-cell acute lymphocytic leukemia protein Organism hsa  Homo sapiens (human) Disease H00002   T-cell acute lymphoblastic leukemia Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:hsa03000]     6887 (TAL2) Transcription factors [BR:hsa03000]  Eukaryotic type   Basic helix-loop-helix (bHLH)    Tal/Twist/Atonal/Hen, Lymphoid factors     6887 (TAL2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  HLH COE1_HLH PMBR Motif Other DBs NCBI-GeneID:  6887 NCBI-ProteinID:  NP_005412 OMIM:  186855 HGNC:  11557 Ensembl:  ENSG00000186051 UniProt:  Q16559 LinkDB All DBs Position 9:105662457..105663124 Genome browser AA seq 108 aa AA seqDB search MTRKIFTNTRERWRQQNVNSAFAKLRKLIPTHPPDKKLSKNETLRLAMRYINFLVKVLGE QSLQQTGVAAQGNILGLFPQGPHLPGLEDRTLLENYQVPSPGPSHHIP NT seq 327 nt NT seq  +upstreamnt  +downstreamnt atgaccaggaagatcttcacaaataccagggagcggtggaggcagcagaatgtcaacagc gcctttgccaagctgaggaagctcatccccactcaccctccagacaaaaagctgagcaaa aatgaaacgcttcgcctggcaatgaggtatatcaacttcttggtcaaggtcttgggggag caaagcctgcaacaaacgggagtggctgctcaggggaacattctggggctcttccctcaa ggaccccacctgccaggcctggaggacagaactctgcttgagaactaccaggttccttca cctggtccaagccaccacattccttag

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