Panthera pardus (leopard): 109245334 Help Entry 109245334         CDS       T06062                                  Symbol CLDN20 Name (RefSeq) claudin-20   KO K06087   claudin Organism ppad  Panthera pardus (leopard) Pathway ppad03272   Virion - Hepatitis viruses ppad04382   Cornified envelope formation ppad04514   Cell adhesion molecule (CAM) interaction ppad04530   Tight junction ppad04670   Leukocyte transendothelial migration ppad05160   Hepatitis C Brite KEGG Orthology (KO) [BR:ppad00001]  09120 Genetic Information Processing   09125 Information processing in viruses    03272 Virion - Hepatitis viruses     109245334 (CLDN20)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecule (CAM) interaction     109245334 (CLDN20)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     109245334 (CLDN20)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     109245334 (CLDN20)   09158 Development and regeneration    04382 Cornified envelope formation     109245334 (CLDN20)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     109245334 (CLDN20)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:ppad03037]     109245334 (CLDN20)    04147 Exosome [BR:ppad04147]     109245334 (CLDN20) Cilium and associated proteins [BR:ppad03037]  Other cilia and associated proteins   Stereociliary proteins    109245334 (CLDN20) Exosome [BR:ppad04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    109245334 (CLDN20)   Exosomal proteins of colorectal cancer cells    109245334 (CLDN20) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  PMP22_Claudin Claudin_2 Motif Other DBs NCBI-GeneID:  109245334 NCBI-ProteinID:  XP_019268197 Ensembl:  ENSPPRG00000017414 UniProt:  A0A9V1DV89 LinkDB All DBs Position Unknown AA seq 219 aa AA seqDB search MASAGLQLLAFVLALSGVSGVLTATLLPNWKVNVDSGSNIITAVVQLQGLWMDCTWYSTG MFSCTLKYSILSLPIHVQAARATMVLACVLSALGICTSTVGMKCTRLGGDGDTKSHASFA GGVCFMAAGVSGLIPTVWYTKEIIANFLDLTVPESNKHEPGGAVYLGFISAALLFVSGMI FCTSCMKKAPEAWLFAAKQRHTSAMQPEGSSAYNLKDYV NT seq 660 nt NT seq  +upstreamnt  +downstreamnt atggcgtccgcgggtctccagctcctggccttcgtcctggctctatctggggtgtctgga gtgctcacggccactctgctgcccaactggaaggtgaacgtggattcgggctccaacatc atcacggccgtcgtgcagctgcaggggctgtggatggactgcacgtggtacagcaccggg atgttcagctgcaccctcaagtactccattctgtccctccccatccacgtgcaggccgca cgggccaccatggtcctggcctgcgtcctgtccgcgttggggatctgcacttccacagtg gggatgaaatgcactcgcttaggaggggacggagacacaaagagccacgcttcttttgcc ggaggagtctgcttcatggctgcaggggtctctggtttaatcccaaccgtgtggtacaca aaggagatcatagcaaacttcctggacctgacggttccagaaagcaacaaacatgagccc ggaggagccgtctacctcggattcatttcggccgcgctgttgttcgtctccggcatgatt ttctgcacttcctgtatgaaaaaggctccggaagcttggctctttgcagccaagcagcgg catacctccgccatgcagccagagggcagctccgcgtacaacctcaaagattacgtgtaa

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