Pan paniscus (bonobo): 100973023 Help Entry 100973023         CDS       T02283                                  Symbol CLDN34 Name (RefSeq) claudin-34 isoform X1   KO K06087   claudin Organism pps  Pan paniscus (bonobo) Pathway pps03272   Virion - Hepatitis viruses pps04382   Cornified envelope formation pps04514   Cell adhesion molecule (CAM) interaction pps04530   Tight junction pps04670   Leukocyte transendothelial migration pps05160   Hepatitis C Brite KEGG Orthology (KO) [BR:pps00001]  09120 Genetic Information Processing   09125 Information processing in viruses    03272 Virion - Hepatitis viruses     100973023 (CLDN34)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecule (CAM) interaction     100973023 (CLDN34)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     100973023 (CLDN34)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     100973023 (CLDN34)   09158 Development and regeneration    04382 Cornified envelope formation     100973023 (CLDN34)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     100973023 (CLDN34)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:pps03037]     100973023 (CLDN34)    04147 Exosome [BR:pps04147]     100973023 (CLDN34) Cilium and associated proteins [BR:pps03037]  Other cilia and associated proteins   Stereociliary proteins    100973023 (CLDN34) Exosome [BR:pps04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    100973023 (CLDN34)   Exosomal proteins of colorectal cancer cells    100973023 (CLDN34) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 Motif Other DBs NCBI-GeneID:  100973023 NCBI-ProteinID:  XP_003811996 Ensembl:  ENSPPAG00000019292 UniProt:  A0A2R8ZI17 LinkDB All DBs Position X:11762676..11773083 Genome browser AA seq 258 aa AA seqDB search MATVLMRTPSCLDQEAGAEELGRTSERSCVHVGPAGQFPGCAATMVWFCNSADCQFSVFA LTTIGWILSSTSTGLVEWRIWYMKDTSLYPPGIACVGIFRVCIYRHRTNSTTTKFCYRYS YQDTFLPFEISMAQRFLLTASIFGFFGRAFNMFALRNMSMRMFEEDTYNSFVVSGILNIA AGVFNLTAVLQNYDAVINSQGITFLPSLQMPFKPDVQEVGTAIQVAGIGVLPMLLTGMFS LFYKCPPYGQVHPGISEM NT seq 777 nt NT seq  +upstreamnt  +downstreamnt atggctaccgtgttgatgagaactcccagctgcctggaccaagaagccggtgctgaagaa ctaggcaggacatccgagaggagctgtgtccatgtcggccccgctggccagtttcctggg tgcgctgccaccatggtctggttctgcaacagtgccgactgccaattttcagtcttcgcc cttaccaccataggatggatcctctcctctacgtccacgggcctcgtggagtggcgaata tggtacatgaaagacacctcgctctacccccctggaatcgcctgcgtgggaatatttaga gtctgcatttaccggcatcgcaccaacagcaccacaaccaaattttgttaccgatacagc taccaggacacctttctcccttttgaaatttccatggctcaacgcttcctactgactgcc agcattttcggattcttcgggagagcctttaacatgtttgcacttagaaacatgtccatg agaatgtttgaggaggacacctacaattcattcgttgtttcaggaattctcaacattgct gctggtgtctttaacttaactgctgtgctccagaactatgatgccgtcataaactcacag gggatcaccttcctgccatctctccaaatgcccttcaagccagatgtgcaggaagttggc actgccattcaagtggcagggataggtgtcttgccgatgctgttaactgggatgttttct ctgttttacaaatgtcccccgtacggccaagtgcatcctggtatttcagaaatgtga

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