Homo sapiens (human): 9074 Help Entry 9074              CDS       T01001                                  Symbol CLDN6 Name (RefSeq) claudin 6   KO K06087   claudin Organism hsa  Homo sapiens (human) Pathway hsa03272   Virion - Hepatitis viruses hsa04514   Cell adhesion molecules hsa04530   Tight junction hsa04670   Leukocyte transendothelial migration hsa05130   Pathogenic Escherichia coli infection hsa05160   Hepatitis C Network nt06180  Pathogenic Escherichia coli   Element N01287   Tight junction-Actin signaling pathway Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09125 Information processing in viruses    03272 Virion - Hepatitis viruses     9074 (CLDN6)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecules     9074 (CLDN6)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     9074 (CLDN6)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     9074 (CLDN6)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     9074 (CLDN6)   09171 Infectious disease: bacterial    05130 Pathogenic Escherichia coli infection     9074 (CLDN6)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     9074 (CLDN6)    04147 Exosome [BR:hsa04147]     9074 (CLDN6) Cilium and associated proteins [BR:hsa03037]  Other cilia and associated proteins   Stereociliary proteins    9074 (CLDN6) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    9074 (CLDN6)   Exosomal proteins of colorectal cancer cells    9074 (CLDN6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 GPDPase_memb Motif Other DBs NCBI-GeneID:  9074 NCBI-ProteinID:  NP_067018 OMIM:  615798 HGNC:  2048 Ensembl:  ENSG00000184697 UniProt:  P56747 LinkDB All DBs Position 16:complement(3014712..3018183) Genome browser AA seq 220 aa AA seqDB search MASAGMQILGVVLTLLGWVNGLVSCALPMWKVTAFIGNSIVVAQVVWEGLWMSCVVQSTG QMQCKVYDSLLALPQDLQAARALCVIALLVALFGLLVYLAGAKCTTCVEEKDSKARLVLT SGIVFVISGVLTLIPVCWTAHAIIRDFYNPLVAEAQKRELGASLYLGWAASGLLLLGGGL LCCTCPSGGSQGPSHYMARYSTSAPAISRGPSEYPTKNYV NT seq 663 nt NT seq  +upstreamnt  +downstreamnt atggcctctgccggaatgcagatcctgggagtcgtcctgacactgctgggctgggtgaat ggcctggtctcctgtgccctgcccatgtggaaggtgaccgctttcatcggcaacagcatc gtggtggcccaggtggtgtgggagggcctgtggatgtcctgcgtggtgcagagcaccggc cagatgcagtgcaaggtgtacgactcactgctggcgctgccacaggacctgcaggctgca cgtgccctctgtgtcatcgccctccttgtggccctgttcggcttgctggtctaccttgct ggggccaagtgtaccacctgtgtggaggagaaggattccaaggcccgcctggtgctcacc tctgggattgtctttgtcatctcaggggtcctgacgctaatccccgtgtgctggacggcg catgccatcatccgggacttctataaccccctggtggctgaggcccaaaagcgggagctg ggggcctccctctacttgggctgggcggcctcaggccttttgttgctgggtggggggttg ctgtgctgcacttgcccctcgggggggtcccagggccccagccattacatggcccgctac tcaacatctgcccctgccatctctcgggggccctctgagtaccctaccaagaattacgtc tga

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