Neogale vison (American mink): 122890038 Help Entry 122890038         CDS       T08764                                  Symbol ANGPT2 Name (RefSeq) angiopoietin-2 isoform X1   KO K05466   angiopoietin 2 Organism nvs  Neogale vison (American mink) Pathway nvs04010   MAPK signaling pathway nvs04014   Ras signaling pathway nvs04015   Rap1 signaling pathway nvs04066   HIF-1 signaling pathway nvs04151   PI3K-Akt signaling pathway nvs05167   Kaposi sarcoma-associated herpesvirus infection Brite KEGG Orthology (KO) [BR:nvs00001]  09130 Environmental Information Processing   09132 Signal transduction    04010 MAPK signaling pathway     122890038 (ANGPT2)    04014 Ras signaling pathway     122890038 (ANGPT2)    04015 Rap1 signaling pathway     122890038 (ANGPT2)    04066 HIF-1 signaling pathway     122890038 (ANGPT2)    04151 PI3K-Akt signaling pathway     122890038 (ANGPT2)  09160 Human Diseases   09172 Infectious disease: viral    05167 Kaposi sarcoma-associated herpesvirus infection     122890038 (ANGPT2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04052 Cytokines and neuropeptides [BR:nvs04052]     122890038 (ANGPT2) Cytokines and neuropeptides [BR:nvs04052]  Cytokines   Growth factors (RTK binding)    122890038 (ANGPT2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Fibrinogen_C Spc29 Motif Other DBs NCBI-GeneID:  122890038 NCBI-ProteinID:  XP_044081656 UniProt:  A0A8C7AQR2 LinkDB All DBs Position 11:206160623..206214129 Genome browser AA seq 495 aa AA seqDB search MWQIVFFTLGCDLVLAAAYNNFRRSMDSIGRRQYQVQHGACSYTFLLPETDNCRPSSSYV PNAVQRDAPLDYDDSVQRLQVLENIMENNTQWLMKLENYIQDNMKREMVEMQQNAVQNQT AVMIEIGTNLLNQTAAQTRKLTDVEAQVLNQTTRLELQLLEHSLSTNKLEKQILDQTSEI NKLQDKNSFLEKKVLDMEDKHIVQLRSIKEEKDQLQVLVSKQNSIIEELEKQLVTATVNN SVLQKQQHDLMETVHNLLSMISTSNSAKNSFDVKEEQVIFRDCAEVFKSGLTANGIYTLT FPNSTEEIKAYCDMETSGGGWTVIQRREDGSVDFQKTWKEYKVGFGNPSGEHWLGNEFVF QVTNQQPYVLKIHLKDWEGNEAYSLYEHFYLSGEELNYRIHLKGLTGTAGKISSISQPGN DFSTKDADNDKCICKCAQMLTGGWWFDACGPSNLNGMYYPQKQNTNKFNGIKWYYWKGSG YSLKATTMMIRPAGF NT seq 1488 nt NT seq  +upstreamnt  +downstreamnt atgtggcagattgttttctttactttgggctgtgatcttgtcctagccgcagcctataac aactttcggagaagcatggacagcatcgggaggaggcagtatcaggttcagcacggagcc tgcagctacaccttcctcctgccagagacagacaactgtcgcccttccagctcctacgtg cccaacgctgtgcagagggacgcaccgctagactacgatgactcggtacagaggctgcaa gtgctggagaacatcatggaaaacaatactcagtggctgatgaagcttgagaattacatc caggacaacatgaagagagaaatggtagagatgcaacagaatgcagtacagaaccagacc gctgtgatgatagaaataggaacaaacctcctcaatcaaacagcagcgcaaacccggaag ctaacggacgttgaagcacaagtattaaatcagacaacaagacttgaacttcagcttctg gaacattccctttccaccaacaaattggaaaaacagattttggatcagaccagtgaaata aacaaattgcaagataagaacagtttcttagaaaagaaagtactagacatggaagacaag catatagttcaactacgatcaataaaagaagagaaagatcagctccaggtattagtatcc aagcaaaattccatcattgaagaactagaaaaacaactggtgactgccacagtgaataac tccgttctccagaagcagcaacacgatctgatggagacagttcataatttattgtctatg atatcaacatcaaactcagccaagaactccttcgatgttaaggaagaacaagtcattttc agagactgtgcagaagtgttcaagtcaggactgacagccaacggcatctacacgctcaca ttccctaattccacagaggagatcaaggcctactgcgacatggaaacctctggaggcggg tggacggtcattcagcggcgtgaagatggcagtgttgattttcagaagacttggaaagaa tataaagtgggatttgggaacccttctggtgaacactggctgggaaatgaattcgttttc caagtcaccaatcaacagccctacgtgcttaaaatacaccttaaagactgggaggggaac gaggcgtactcactgtatgaacatttctatctctccggtgaagaacttaattacaggatt caccttaaaggacttacagggacggccggcaaaataagcagcataagccaaccaggaaat gattttagcacaaaggatgcagacaacgacaaatgtatttgcaaatgtgcacaaatgctc acaggaggctggtggtttgatgcatgcggtccgtccaacttgaacggaatgtactacccg cagaagcagaacacaaataagttcaacggtattaagtggtactactggaaaggctccggc tactcgctcaaggccacgaccatgatgatccgcccagcaggtttctag

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