Homo sapiens (human): 24146 Help Entry 24146             CDS       T01001                                  Symbol CLDN15 Name (RefSeq) claudin 15   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     24146 (CLDN15)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecules     24146 (CLDN15)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     24146 (CLDN15)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     24146 (CLDN15)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     24146 (CLDN15)   09171 Infectious disease: bacterial    05130 Pathogenic Escherichia coli infection     24146 (CLDN15)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     24146 (CLDN15)    04147 Exosome [BR:hsa04147]     24146 (CLDN15) Cilium and associated proteins [BR:hsa03037]  Other cilia and associated proteins   Stereociliary proteins    24146 (CLDN15) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    24146 (CLDN15)   Exosomal proteins of colorectal cancer cells    24146 (CLDN15) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 Motif Other DBs NCBI-GeneID:  24146 NCBI-ProteinID:  NP_001172009 OMIM:  615778 HGNC:  2036 Ensembl:  ENSG00000106404 UniProt:  P56746 LinkDB All DBs Position 7:complement(101232094..101238820) Genome browser AA seq 228 aa AA seqDB search MSMAVETFGFFMATVGLLMLGVTLPNSYWRVSTVHGNVITTNTIFENLWFSCATDSLGVY NCWEFPSMLALSGYIQACRALMITAILLGFLGLLLGIAGLRCTNIGGLELSRKAKLAATA GALHILAGICGMVAISWYAFNITRDFFDPLYPGTKYELGPALYLGWSASLISILGGLCLC SACCCGSDEDPAASARRPYQAPVSVMPVATSDQEGDSSFGKYGRNAYV NT seq 687 nt NT seq  +upstreamnt  +downstreamnt atgtcgatggctgtggaaacctttggcttcttcatggcaactgtggggctgctgatgctg ggggtgactctgccaaacagctactggcgagtgtccactgtgcacgggaacgtcatcacc accaacaccatcttcgagaacctctggtttagctgtgccaccgactccctgggcgtctac aactgctgggagttcccgtccatgctggccctctctgggtatattcaggcctgccgggca ctcatgatcaccgccatcctcctgggcttcctcggcctcttgctaggcatagcgggcctg cgctgcaccaacattgggggcctggagctctccaggaaagccaagctggcggccaccgca ggggccctccacattctggccggtatctgcgggatggtggccatctcctggtacgccttc aacatcacccgggacttcttcgaccccttgtaccccggaaccaagtacgagctgggcccc gccctctacctggggtggagcgcctcactgatctccatcctgggtggcctctgcctctgc tccgcctgctgctgcggctctgacgaggacccagccgccagcgcccggcggccctaccag gctccagtgtccgtgatgcccgtcgccacctcggaccaagaaggcgacagcagctttggc aaatacggcagaaacgcctacgtgtag

DBGET integrated database retrieval system