Homo sapiens (human): 23786 Help Entry 23786             CDS       T01001                                  Symbol BCL2L13, BCL-RAMBO, Bcl2-L-13, MIL1 Name (RefSeq) BCL2 like 13   KO K15485   Bcl-2-like protein 13 Organism hsa  Homo sapiens (human) Pathway hsa04137   Mitophagy - animal hsa05134   Legionellosis Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09141 Transport and catabolism    04137 Mitophagy - animal     23786 (BCL2L13)  09160 Human Diseases   09171 Infectious disease: bacterial    05134 Legionellosis     23786 (BCL2L13) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Bcl-2 CEND1 Motif Other DBs NCBI-GeneID:  23786 NCBI-ProteinID:  NP_056182 OMIM:  619822 HGNC:  17164 Ensembl:  ENSG00000099968 UniProt:  Q9BXK5 LinkDB All DBs Position 22:17628877..17730855 Genome browser AA seq 485 aa AA seqDB search MASSSTVPLGFHYETKYVVLSYLGLLSQEKLQEQHLSSPQGVQLDIASQSLDQEILLKVK TEIEEELKSLDKEISEAFTSTGFDRHTSPVFSPANPESSMEDCLAHLGEKVSQELKEPLH KALQMLLSQPVTYQAFRECTLETTVHASGWNKILVPLVLLRQMLLELTRRGQEPLSALLQ FGVTYLEDYSAEYIIQQGGWGTVFSLESEEEEYPGITAEDSNDIYILPSDNSGQVSPPES PTVTTSWQSESLPVSLSASQSWHTESLPVSLGPESWQQIAMDPEEVKSLDSNGAGEKSEN NSSNSDIVHVEKEEVPEGMEEAAVASVVLPARELQEALPEAPAPLLPHITATSLLGTREP DTEVITVEKSSPATSLFVELDEEEVKAATTEPTEVEEVVPALEPTETLLSEKEINAREES LVEELSPASEKKPVPPSEGKSRLSPAGEMKPMPLSEGKSILLFGGAAAVAILAVAIGVAL ALRKK NT seq 1458 nt NT seq  +upstreamnt  +downstreamnt atggcgtcctcttctactgtgcctctgggatttcactatgaaacaaagtatgttgttctc agctacttgggactcctctctcaagagaagctgcaagagcaacatctttcctcaccccaa ggggttcaactagatatagcttcacaatctctggatcaagaaattttattaaaagttaaa actgaaattgaagaagagctaaaatctctggacaaagaaatttctgaagccttcaccagc acaggctttgaccgtcacacttctccagtgttcagccctgccaatccagaaagctcaatg gaagactgcttggcccatcttggagaaaaagtgtcccaggaactgaaagagcctctccat aaagcattgcaaatgctcctgagccagccagtgacatatcaggcatttcgggaatgtaca ctggagaccacagttcatgccagcggctggaataagattttggtgcctctggttttgcta cgacaaatgcttttggaattgacaagacgtggtcaagaacctttgagcgcactgctgcag tttggcgtgacatacctggaggactattcggcagagtacatcattcagcaaggtggctgg ggcactgtgtttagtcttgagtcagaggaggaggaataccctggaatcactgcagaagat agcaatgacatttacatcctgcccagcgacaactctggacaagtcagtcccccagagtct ccaactgtgaccacttcctggcagtctgagagcttacctgtgtcactgtcagctagccag agttggcacacagaaagcctgccagtgtcactaggccctgagtcctggcagcagattgca atggatcctgaagaagtgaaaagcttagacagcaacggagctggagagaagagtgagaac aactcctctaattctgacattgtgcacgtggagaaagaagaggtgcccgagggcatggaa gaggctgctgtggcttctgtggtcttgccagcgcgggagctgcaagaggcacttcctgaa gccccagctcccttgcttccacatatcactgccacctccctgctggggacaagggaacct gacacagaagtgatcacagttgagaaatccagccctgctacatctctgtttgtagaactt gatgaagaagaggtgaaagcagcaacaactgaacctactgaagtggaggaggtggtcccc gcactggaacccacagaaacgctgctgagtgagaaggagataaacgcaagggaagagagc cttgtggaagagctgtcccctgccagcgagaagaagcccgtgccgccgtctgagggcaag tctagactgtcccccgccggtgagatgaagcccatgccgctgtctgagggcaagtctata ctgctgtttggaggggctgctgctgttgccatcctggcagtggccatcggggtagccctg gctctgagaaagaaatag

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