Pan paniscus (bonobo): 100989187 Help Entry 100989187         CDS       T02283                                  Symbol CLDN7 Name (RefSeq) claudin-7   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     100989187 (CLDN7)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecule (CAM) interaction     100989187 (CLDN7)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     100989187 (CLDN7)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     100989187 (CLDN7)   09158 Development and regeneration    04382 Cornified envelope formation     100989187 (CLDN7)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     100989187 (CLDN7)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:pps03037]     100989187 (CLDN7)    04147 Exosome [BR:pps04147]     100989187 (CLDN7) Cilium and associated proteins [BR:pps03037]  Other cilia and associated proteins   Stereociliary proteins    100989187 (CLDN7) Exosome [BR:pps04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    100989187 (CLDN7)   Exosomal proteins of colorectal cancer cells    100989187 (CLDN7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 DUF7847 Clc-like Motif Other DBs NCBI-GeneID:  100989187 NCBI-ProteinID:  XP_008960712 Ensembl:  ENSPPAG00000035150 UniProt:  A0A2R9B348 LinkDB All DBs Position 19:complement(14852538..14855530) Genome browser AA seq 211 aa AA seqDB search MANSGLQLLGFSMALLGWVGLVACTAIPQWQMSSYAGDNIITAQAMYKGLWMDCVTQSTG MMSCKMYDSVLALSAALQATRALMVVSLVLGFLAMFVATMGMKCTRCGGDDKVKKARIAM GGGIIFIVAGLAALVACSWYGHQIVTDFYNPLIPTNIKYEFGPAIFIGWAGSALVILGGA LLSCSCPGNESKAGYRAPRSYPKSNSSKEYV NT seq 636 nt NT seq  +upstreamnt  +downstreamnt atggccaattcgggcctgcagttgctgggcttctccatggccctgctgggctgggtgggt ctggtggcctgcaccgccatcccgcagtggcagatgagctcctatgcgggtgacaacatc atcacggcccaggccatgtacaaggggctgtggatggactgcgttacgcagagcacgggg atgatgagctgcaaaatgtacgactcggtgctcgccctgtccgcggccttgcaggccact cgagccctaatggtggtctccctggtgctgggcttcctggccatgtttgtggccacgatg ggcatgaagtgcacgcgctgtgggggagacgacaaagtgaagaaggcccgtatagccatg ggtggaggcataattttcatcgtggcaggtcttgccgccttggtagcttgctcctggtat ggccatcagattgtcacagacttttataaccctttgatccctaccaacattaagtatgag tttggccctgccatctttattggctgggcagggtctgccctagtcatcctgggaggtgca ctgctctcctgttcctgtcctgggaatgagagcaaggctgggtaccgtgcaccccgctct taccctaagtccaactcttccaaggagtatgtgtga

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