Pan paniscus (bonobo): 100975921 Help Entry 100975921         CDS       T02283                                  Symbol CLDN18 Name (RefSeq) claudin-18   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     100975921 (CLDN18)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecule (CAM) interaction     100975921 (CLDN18)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     100975921 (CLDN18)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     100975921 (CLDN18)   09158 Development and regeneration    04382 Cornified envelope formation     100975921 (CLDN18)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     100975921 (CLDN18)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:pps03037]     100975921 (CLDN18)    04147 Exosome [BR:pps04147]     100975921 (CLDN18) Cilium and associated proteins [BR:pps03037]  Other cilia and associated proteins   Stereociliary proteins    100975921 (CLDN18) Exosome [BR:pps04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    100975921 (CLDN18)   Exosomal proteins of colorectal cancer cells    100975921 (CLDN18) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 Motif Other DBs NCBI-GeneID:  100975921 NCBI-ProteinID:  XP_003822533 Ensembl:  ENSPPAG00000004749 UniProt:  A0A2R8Z890 LinkDB All DBs Position 2:135915550..135936176 Genome browser AA seq 261 aa AA seqDB search MSTTTCQVVAFLLSILGLAGCIAATGMDMWSTQDLYDNPVTSVFQYEGLWRSCVRQSSGF TECRPYFTILGLPAMLQAVRALMIVGIVLGAIGLLVSIFALKCIRIGSMEDSAKANMTLT SGIMFIVSGLCAIAGVSVFANMLVTNFWMSTANMYTGMGGMVQTVQTRYTFGAALFVGWV AGGLTLIGGVMMCIACRGLAPEETNYKAVSYHASGHSAAYKPGGFKASTGFGSNTKNKKI YDGGARTEDEVQSYPSKHDYV NT seq 786 nt NT seq  +upstreamnt  +downstreamnt atgtccaccaccacatgccaagtggtggcgttcctcctgtccatcctggggctggccggc tgcatcgcggccaccgggatggacatgtggagcacccaggacctgtacgacaaccccgtc acctccgtgttccagtacgaagggctctggaggagctgcgtgaggcagagttcaggcttc accgaatgcaggccctatttcaccatcctgggccttccagccatgctgcaggcagtgcga gccctgatgatcgtaggcatcgtcctgggtgccattggcctcctggtatccatctttgcc ctgaaatgcatccgcattggcagcatggaggactctgccaaagccaacatgacactgacc tccgggatcatgttcattgtctcaggtctttgtgcaattgctggagtgtctgtgtttgcc aacatgctggtgactaacttctggatgtccacagctaacatgtacaccggcatgggtggg atggtgcagactgttcagaccaggtacacatttggtgcggctctgttcgtgggctgggtc gctggaggcctcacactaattgggggtgtgatgatgtgcatcgcctgccggggcctggca ccagaagaaaccaactacaaagccgtttcttatcatgcctcgggccacagtgctgcctac aagcctggaggcttcaaggccagcactggctttggatccaacaccaaaaacaagaagata tacgatggaggtgcccgcacagaggacgaggtacaatcttatccttccaagcacgactat gtgtaa

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