Pan troglodytes (chimpanzee): 460082 Help Entry 460082            CDS       T01005                                  Symbol SEPTIN2 Name (RefSeq) septin-2 isoform X2   KO K16942   septin 2 Organism ptr  Pan troglodytes (chimpanzee) Pathway ptr05100   Bacterial invasion of epithelial cells Brite KEGG Orthology (KO) [BR:ptr00001]  09160 Human Diseases   09171 Infectious disease: bacterial    05100 Bacterial invasion of epithelial cells     460082 (SEPTIN2)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04131 Membrane trafficking [BR:ptr04131]     460082 (SEPTIN2)   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:ptr03037]     460082 (SEPTIN2)    04812 Cytoskeleton proteins [BR:ptr04812]     460082 (SEPTIN2)    04147 Exosome [BR:ptr04147]     460082 (SEPTIN2) Membrane trafficking [BR:ptr04131]  Exocytosis   Calcium ion-dependent exocytosis    Septins     460082 (SEPTIN2) Cilium and associated proteins [BR:ptr03037]  Motile cilia and associated proteins   Sperm associated proteins    460082 (SEPTIN2) Cytoskeleton proteins [BR:ptr04812]  Eukaryotic cytoskeleton proteins   Septins    Septins     Group 2      460082 (SEPTIN2) Exosome [BR:ptr04147]  Exosomal proteins   Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)    460082 (SEPTIN2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Septin MMR_HSR1 GTP_EFTU RsgA_GTPase Dynamin_N Ras AIG1 AAA_22 ABC_tran AAA_16 Roc AAA_29 Motif Other DBs NCBI-GeneID:  460082 NCBI-ProteinID:  XP_024210499 Ensembl:  ENSPTRG00000023481 VGNC:  2812 LinkDB All DBs Position 13:143620386..143658595 Genome browser AA seq 321 aa AA seqDB search MVVGESGLGKSTLINSLFLTDLYPERVIPGAAEKIERTVQIEASTVEIEERGVKLRLTVV DTPGYGDAINCRDCFKTIISYIDEQFERYLHDESGLNRRHIIDNRVHCCFYFISPFGHGL KPLDVAFMKAIHNKVNIVPVIAKADTLTLKERERLKKRILDEIEEHNIKIYHLPDAESDE DEDFKEQTRLLKASIPFSVVGSNQLIEAKGKKVRGRLYPWGVVEVENPEHNDFLKLRTML ITHMQDLQEVTQDLHYENFRSERLKRGGRKVENEDMNKDQILLEKEAELRRMQEMIARMQ AQMQMQMQGGDGDGGALGHHV NT seq 966 nt NT seq  +upstreamnt  +downstreamnt atggtggtcggtgaatcaggtctaggaaaatcgactctcataaacagcctattcctaact gatctgtacccagaaagagtcatacctggagcagcagaaaaaattgaaagaaccgtccag attgaggcttcaactgttgaaattgaagagcgaggggtcaagctacgcctgacagtggta gatacccctggctatggtgacgctatcaactgcagagattgttttaagacaattatctcc tatattgatgagcaatttgagaggtacctgcatgacgagagcggcttgaacaggcggcac atcattgataatagggtgcattgttgcttttactttatttcaccttttggacatggactt aagcccttagatgtggcgtttatgaaggcaatacacaacaaggtgaatattgtgcctgtc attgcaaaagctgacactctcaccctgaaggaacgggagcggctgaagaaaaggattctg gatgaaattgaagaacataacatcaaaatctatcacttacctgatgcagaatcagatgaa gatgaagattttaaagagcagactagacttctcaaagctagcatcccattctctgtggtt ggatccaatcagttgattgaagccaaaggaaagaaggtcagaggccgcctctacccctgg ggtgttgtggaggtggagaacccagagcacaatgactttctgaagctgagaaccatgctc atcacccacatgcaggatctccaggaggtgacccaggaccttcattatgaaaacttccgt tctgagagactcaagagaggcggcaggaaagtggagaatgaggacatgaataaagaccag atcttgctggaaaaagaagctgagctccgccgcatgcaagagatgattgcaaggatgcaa gcacagatgcagatgcagatgcagggcggggatggcgatggcggggctctcgggcaccac gtgtaa

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