Puma concolor (puma): 112861398 Help Entry 112861398         CDS       T08890                                  Symbol CLDN10 Name (RefSeq) claudin-10 isoform X1   KO K06087   claudin Organism pcoo  Puma concolor (puma) Pathway pcoo03272   Virion - Hepatitis viruses pcoo04382   Cornified envelope formation pcoo04514   Cell adhesion molecule (CAM) interaction pcoo04530   Tight junction pcoo04670   Leukocyte transendothelial migration pcoo05160   Hepatitis C Brite KEGG Orthology (KO) [BR:pcoo00001]  09120 Genetic Information Processing   09125 Information processing in viruses    03272 Virion - Hepatitis viruses     112861398 (CLDN10)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecule (CAM) interaction     112861398 (CLDN10)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     112861398 (CLDN10)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     112861398 (CLDN10)   09158 Development and regeneration    04382 Cornified envelope formation     112861398 (CLDN10)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     112861398 (CLDN10)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:pcoo03037]     112861398 (CLDN10)    04147 Exosome [BR:pcoo04147]     112861398 (CLDN10) Cilium and associated proteins [BR:pcoo03037]  Other cilia and associated proteins   Stereociliary proteins    112861398 (CLDN10) Exosome [BR:pcoo04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    112861398 (CLDN10)   Exosomal proteins of colorectal cancer cells    112861398 (CLDN10) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  PMP22_Claudin Claudin_2 Clc-like Motif Other DBs NCBI-GeneID:  112861398 NCBI-ProteinID:  XP_025780550 UniProt:  A0A6P6HXJ5 LinkDB All DBs Position Unknown AA seq 229 aa AA seqDB search MSRAQISALVFGVGGFGALVAATASNEWKVTTRASSVITATWVYQGLWMNCAGNALGSFH CRPHFTIFKVEGYIQACRGLMIAAVSLGFFGSIFALFGMKCTKVGGSDKAKAKIACLAGI VFILSGLCSMTGCSLYANKITTEFFDPLYVEQKYELGAALFIGWAGASLCIIGGVIFCFS ISDNNKTPRMGYAYNGATSVMSSRTKYPGAGGDLKTTNPSKQFDKNAYV NT seq 690 nt NT seq  +upstreamnt  +downstreamnt atgtccagggcgcagatctcagctctggtgtttggcgtcggagggtttggagctcttgtc gcggccaccgcgtccaatgaatggaaagtgaccacccgagcatcatcggtgataaccgcc acttgggtttaccagggtctgtggatgaactgcgcaggtaacgcgttgggttctttccat tgccgaccacactttactatcttcaaagtagaaggttatatccaggcatgtagaggactt atgattgccgctgtcagtctgggcttttttggttccatatttgccctgtttggaatgaag tgtaccaaagtcggaggctcagataaagccaaagctaaaattgcttgtttggctggaatt gtattcatactgtcagggttgtgctcaatgaccggttgttccctctacgcaaacaaaatc acaacggaattctttgatcctctctatgttgagcagaagtatgaattaggagctgctctg tttattggatgggcgggagcctcactctgcataattggtggtgtcatattttgcttttca atatctgacaacaacaaaacacccagaatgggatacgcatacaacggggccacatctgtc atgtcttctcggacgaaatatcctggcgcaggaggagatcttaaaaccacaaacccttca aaacagtttgataaaaacgcttatgtctga

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