Neogale vison (American mink): 122915099 Help Entry 122915099         CDS       T08764                                  Symbol BCL2L11 Name (RefSeq) bcl-2-like protein 11 isoform X1   KO K16341   Bcl-2-like protein 11 Organism nvs  Neogale vison (American mink) Pathway nvs01521   EGFR tyrosine kinase inhibitor resistance nvs04068   FoxO signaling pathway nvs04151   PI3K-Akt signaling pathway nvs04210   Apoptosis nvs04215   Apoptosis - multiple species nvs04932   Non-alcoholic fatty liver disease nvs05169   Epstein-Barr virus infection nvs05200   Pathways in cancer nvs05206   MicroRNAs in cancer nvs05210   Colorectal cancer Brite KEGG Orthology (KO) [BR:nvs00001]  09130 Environmental Information Processing   09132 Signal transduction    04068 FoxO signaling pathway     122915099 (BCL2L11)    04151 PI3K-Akt signaling pathway     122915099 (BCL2L11)  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     122915099 (BCL2L11)    04215 Apoptosis - multiple species     122915099 (BCL2L11)  09160 Human Diseases   09161 Cancer: overview    05200 Pathways in cancer     122915099 (BCL2L11)    05206 MicroRNAs in cancer     122915099 (BCL2L11)   09162 Cancer: specific types    05210 Colorectal cancer     122915099 (BCL2L11)   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     122915099 (BCL2L11)   09167 Endocrine and metabolic disease    04932 Non-alcoholic fatty liver disease     122915099 (BCL2L11)   09176 Drug resistance: antineoplastic    01521 EGFR tyrosine kinase inhibitor resistance     122915099 (BCL2L11) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Bclx_interact Bim_N Motif Other DBs NCBI-GeneID:  122915099 NCBI-ProteinID:  XP_044117560 LinkDB All DBs Position 8:complement(108272710..108318028) Genome browser AA seq 288 aa AA seqDB search MFPAAAAGAARARGAARGALGCRTARGGGRAASGRLCAAPGALKASPGLCLPRFFRADGQ GAPGRRRTRAGRRGARARTRRSEGKGRTKKDQMAKQPSDVSSECDREGGQLQPVERPPQL RPGAPTSLQTEQQGNPEGEGDRCPQGSPQGPLAPPASPGPFATRSPLFIFVRRSSLLSRS SSGYFSFDTDRSPAPMSCDKSTQTPSPPCQAFNHYLSAMASRRQSQAVPADMRPEMWIAQ ELRRIGDEFNAYYPRRVFLNNYPAAEAHPQMIILRLLRYIIRLVWRLQ NT seq 867 nt NT seq  +upstreamnt  +downstreamnt atgttcccggcggcggcggccggggcagcgcgggccagaggcgcggcgcgcggagccctc ggctgccggacggcgcgcggcggcgggcgggctgccagtggccggctctgcgctgccccg ggggctctgaaggcgagtcccgggctttgtctcccgcgcttctttcgtgctgacggtcag ggagctccgggtcggcgaaggacgcgggcgggacgccgcggggctcgggcccggacgcga cggtcggaagggaaggggcggacaaaaaaagaccaaatggcaaagcaaccttcagatgta agttctgagtgtgaccgagaaggtggacaattgcagcctgttgagaggcctcctcagctc aggcctggggcccctacctctctacagacagagcagcaaggtaatcctgaaggcgaaggg gaccgctgcccccaaggcagccctcagggcccactggccccacctgccagccccggccct tttgctaccagatccccgcttttcatctttgtgagaagatcctccctgctgtctcgatcc tccagtgggtatttctcttttgacacagacaggagcccggcacccatgagttgtgacaaa tcaacacaaaccccaagtcctccttgccaggccttcaaccattatctcagtgcaatggct tccaggaggcagtctcaggctgtacctgcagatatgcgcccggagatgtggattgcgcag gagttgcggcgtattggagacgagtttaatgcatattacccaaggagggtctttttgaat aattacccagcagcagaagcccacccccaaatgattatcttacgactgttacgttacatc atccgcctggtgtggagattgcagtga

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