Puma concolor (puma): 112870009 Help Entry 112870009         CDS       T08890                                  Name (RefSeq) putative claudin-24   KO K06087   claudin Organism pcoo  Puma concolor (puma) Pathway pcoo03272   Virion - Hepatitis viruses pcoo04382   Cornified envelope formation pcoo04514   Cell adhesion molecules 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     112870009  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecules     112870009  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     112870009  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     112870009   09158 Development and regeneration    04382 Cornified envelope formation     112870009  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     112870009  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:pcoo03037]     112870009    04147 Exosome [BR:pcoo04147]     112870009    04515 Cell adhesion molecules [BR:pcoo04515]     112870009 Cilium and associated proteins [BR:pcoo03037]  Other cilia and associated proteins   Stereociliary proteins    112870009 Exosome [BR:pcoo04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    112870009   Exosomal proteins of colorectal cancer cells    112870009 Cell adhesion molecules [BR:pcoo04515]  Immunoglobulin superfamily   L1 family    112870009 BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  PMP22_Claudin Claudin_2 ABC_membrane_3 Motif Other DBs NCBI-GeneID:  112870009 NCBI-ProteinID:  XP_025788863 UniProt:  A0A6P6IPN0 LinkDB All DBs Position Unknown AA seq 257 aa AA seqDB search MAKAYIPGSIGPKRSRYCEARKTGTPTGVAKVVRLVAMALVFRVATQLVGLSLSLLGWVL SIITTYLPHWKNLNLDLNEMENWTMGLWQACVVQEEVGRQCKDFESFLALPAELRISRIL MFLSNGLGLLGLLASGFGLDCLRVGETRPGLKKGLLILGGTVFWAAGVATLVPVSWVAHV TVQEFWDETMPEIVPRWEFGEALFLGWSAGFSLLLGGCLLNCVACTTQAAPAPGPYAVAE MQIQCLYLENGTADPRV NT seq 774 nt NT seq  +upstreamnt  +downstreamnt atggccaaagcttatattccgggcagcataggaccaaaacggtcacgctactgtgaagca cgaaagacagggactcccacaggggtggccaaagttgtaagacttgttgcaatggctcta gtctttagagtggcgacgcagctcgttggactttcgttatctttgctgggatgggttttg tccattattacaacttacctgccacattggaaaaacctcaatttggacttaaacgagatg gagaactggaccatgggactctggcaggcctgtgtcgtccaagaggaggtggggagacaa tgcaaggactttgaatccttcctggctttgcctgccgaactcaggatctccaggatctta atgttcctgtccaacgggctggggctcctgggcctgctggcctccgggttcggcctggac tgcttgagggtcggagagacgcggccaggcctcaagaagggactgctgatcctgggaggg accgtgttctgggcagcaggcgtcgcgaccctggttccggtctcctgggtcgcccacgtg accgtccaggagttctgggatgagaccatgccagagattgtgcccaggtgggagtttggg gaagccctctttctgggctggtctgctgggttttccctcctcctgggaggctgcctgctg aactgcgtggcctgtactacccaggccgctccggctccgggcccctatgcggtggcagaa atgcaaattcagtgtctgtacctggaaaatggaactgcagacccgagagtgtaa

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