Panthera pardus (leopard): 109248354 Help Entry 109248354         CDS       T06062                                  Name (RefSeq) putative claudin-24   KO K06087   claudin Organism ppad  Panthera pardus (leopard) Pathway ppad03272   Virion - Hepatitis viruses ppad04382   Cornified envelope formation ppad04514   Cell adhesion molecules 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     109248354  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecules     109248354  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     109248354  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     109248354   09158 Development and regeneration    04382 Cornified envelope formation     109248354  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     109248354  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:ppad03037]     109248354    04147 Exosome [BR:ppad04147]     109248354    04515 Cell adhesion molecules [BR:ppad04515]     109248354 Cilium and associated proteins [BR:ppad03037]  Other cilia and associated proteins   Stereociliary proteins    109248354 Exosome [BR:ppad04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    109248354   Exosomal proteins of colorectal cancer cells    109248354 Cell adhesion molecules [BR:ppad04515]  Immunoglobulin superfamily   L1 family    109248354 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  PMP22_Claudin Claudin_2 TMEM37 Motif Other DBs NCBI-GeneID:  109248354 NCBI-ProteinID:  XP_019273563 UniProt:  A0A9V1E3S3 LinkDB All DBs Position Unknown AA seq 219 aa AA seqDB search MTSGVLRLVENAGLLGSLAGQVCSLVTLCIPQWLTLSSGLLESEKYTLGLWETCVTQDTG GRVCQASASLRDLATEMLVARILMCGACVAGSLGLVAVLLGLTCVRYGGHQGSSLERSTN IAGGALFFLAGLATLVPVSYIARVTVQRFWGPEFPTDVPRWDYGSAMFSGWIGGFFLLTG GLLLIASQLCANRLAEKPTSFPSKLDFSRKVPFAKVDFV NT seq 660 nt NT seq  +upstreamnt  +downstreamnt atgacgagtggggtgctccgcctggtcgagaacgcggggctcttgggctccctggctggc caggtgtgctccctggtgacgctctgcatccctcagtggctgaccctctcctcgggctta ctggagagtgagaagtacacgctgggcctgtgggaaacgtgtgtgactcaagacacgggt ggccgtgtgtgccaggcctctgccagcctgcgggacctggccaccgaaatgctggtggcc cgcatcctcatgtgtggcgcctgtgtcgctggctcgctcgggctggtggccgtccttctg ggactgacatgtgtgaggtacgggggccaccagggaagctctttggagagaagcacgaac attgcagggggagctctgttcttcctcgctggactcgccactttggtgcccgtgtcctac atcgcccgggtcaccgtgcagaggttctggggccctgagttcccaaccgacgtgccccgg tgggactatggcagtgccatgttcagcggctggattggcggatttttccttttgaccgga ggccttcttctgatcgcgtcacagctttgtgccaacagattggctgaaaaacccacctct tttccttcaaaactggacttctcaagaaaagtgccttttgctaaggtagactttgtttaa

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