Pan paniscus (bonobo): 100996190 Help Entry 100996190         CDS       T02283                                  Symbol CLDN19 Name (RefSeq) claudin-19 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     100996190 (CLDN19)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecule (CAM) interaction     100996190 (CLDN19)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     100996190 (CLDN19)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     100996190 (CLDN19)   09158 Development and regeneration    04382 Cornified envelope formation     100996190 (CLDN19)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     100996190 (CLDN19)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:pps03037]     100996190 (CLDN19)    04147 Exosome [BR:pps04147]     100996190 (CLDN19) Cilium and associated proteins [BR:pps03037]  Other cilia and associated proteins   Stereociliary proteins    100996190 (CLDN19) Exosome [BR:pps04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    100996190 (CLDN19)   Exosomal proteins of colorectal cancer cells    100996190 (CLDN19) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 Amastin Mntp TMEM127 Motif Other DBs NCBI-GeneID:  100996190 NCBI-ProteinID:  XP_003812921 Ensembl:  ENSPPAG00000039606 UniProt:  A0A2R9BYC0 LinkDB All DBs Position 1:184071444..184081619 Genome browser AA seq 224 aa AA seqDB search MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGLWMSCASQSTG QVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLSVVGMKCTRVGDSNPIAKGRVAI AGGALFILAGLCTLTAVSWYATLVTQEFFNPSTPVNARYEFGPALFVGWASAGLAVLGGS FLCCTCPEPERPNSSPQPYRPGPSAAAREPVVKLPASAKGPLGV NT seq 675 nt NT seq  +upstreamnt  +downstreamnt atggccaactcaggcctccagctcctgggctacttcttggccctgggtggctgggtgggc atcattgctagcacagccctgccacagtggaagcagtcttcctacgcaggcgacgccatc atcactgccgtgggcctctatgaagggctctggatgtcctgcgcctcccagagcactggg caagtgcagtgcaagctctacgactcgctgctcgccctggacggtcacatccaatcagcg cgggccctgatggtggtggcagtgctcctgggcttcgtggccatggtcctcagcgtagtt ggcatgaagtgtacacgggtgggagacagcaaccccattgccaagggccgtgtcgccatc gccgggggagccctcttcatcctggcaggcctctgcactttgactgctgtctcgtggtat gccaccctggtgacccaggagttcttcaacccaagcacacctgtcaatgccaggtatgaa tttggcccagccctgttcgtgggctgggcctcagctggcctggccgtgctgggcggctcc ttcctctgctgcacatgcccggaaccagagagacccaacagcagcccacagccctatcgg cctggaccctctgctgctgcccgagaaccagttgttaaattgcccgcctccgccaagggc cccctgggtgtgtaa

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