Neogale vison (American mink): 122908913 Help Entry 122908913         CDS       T08764                                  Symbol CLDN18 Name (RefSeq) claudin-18 isoform X1   KO K06087   claudin Organism nvs  Neogale vison (American mink) Pathway nvs03272   Virion - Hepatitis viruses nvs04382   Cornified envelope formation nvs04514   Cell adhesion molecules nvs04530   Tight junction nvs04670   Leukocyte transendothelial migration nvs05160   Hepatitis C Brite KEGG Orthology (KO) [BR:nvs00001]  09120 Genetic Information Processing   09125 Information processing in viruses    03272 Virion - Hepatitis viruses     122908913 (CLDN18)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecules     122908913 (CLDN18)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     122908913 (CLDN18)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     122908913 (CLDN18)   09158 Development and regeneration    04382 Cornified envelope formation     122908913 (CLDN18)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     122908913 (CLDN18)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:nvs03037]     122908913 (CLDN18)    04147 Exosome [BR:nvs04147]     122908913 (CLDN18) Cilium and associated proteins [BR:nvs03037]  Other cilia and associated proteins   Stereociliary proteins    122908913 (CLDN18) Exosome [BR:nvs04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    122908913 (CLDN18)   Exosomal proteins of colorectal cancer cells    122908913 (CLDN18) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 Motif Other DBs NCBI-GeneID:  122908913 NCBI-ProteinID:  XP_044108229 LinkDB All DBs Position 6:complement(126081293..126109878) Genome browser AA seq 261 aa AA seqDB search MSTTTCQVVGFLLSLLGLAGCIAATGMDMWSTQDLYDNPVTSVFQYEGLWRSCVRQSSGF TECRPYFTILGLPAMLQAVRALMIVGIVLGAISLLVSIFALKCIRIGSMEDAAKANMTLT SGIMFIISGLCAIVGVSVFANMLVTNFWMSTANMYTGMGGMVQTVQTRYTFGSALFVGWV AGGLTLIGGVMMCIACRGLAPEETNYKAVSYHASGHNVAYKPGGFKASTAFGPNSRNKKI YDGGARTEDEVQSHPSKYDYV NT seq 786 nt NT seq  +upstreamnt  +downstreamnt atgtccaccaccacatgccaagtggtgggcttcctcctgtccctcctgggcctggccggc tgcatcgccgccacggggatggacatgtggagcacccaggacctgtatgacaaccccgtc acctctgtgttccagtacgaggggctctggcggagctgcgtgaggcagagctcagggttc accgagtgccggccctacttcaccatcctaggccttccagccatgctgcaagcagtgcga gccctgatgatcgtgggcattgtcctgggtgccatcagccttctggtgtccatctttgcc ctgaagtgtatccgcattggcagcatggaggatgccgccaaagccaacatgacattgacc tctgggatcatgttcatcatctcaggtctctgtgcaatcgttggagtatctgtatttgcc aacatgctggttaccaacttctggatgtctacagctaacatgtacaccggcatgggtggg atggtgcagaccgttcagaccaggtacacctttggttcggctttgttcgtgggttgggtc gctggaggcctcacactaattgggggtgtgatgatgtgcattgcctgccggggcctggcg cctgaggaaaccaactacaaagctgtgtcttatcatgcctcaggccacaacgtcgcctat aagcccggaggcttcaaggccagcactgcctttgggcccaatagcagaaacaagaagata tacgatgggggtgcccgaacagaggacgaggtacagtctcatccttccaagtacgactac gtgtag

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