Neogale vison (American mink): 122910336 Help Entry 122910336         CDS       T08764                                  Symbol CLDN17 Name (RefSeq) claudin-17   KO K06087   claudin Organism nvs  Neogale vison (American mink) Pathway nvs03272   Virion - Hepatitis viruses nvs04382   Cornified envelope formation nvs04514   Cell adhesion molecules nvs04530   Tight junction nvs04670   Leukocyte transendothelial migration nvs05160   Hepatitis C Brite KEGG Orthology (KO) [BR:nvs00001]  09120 Genetic Information Processing   09125 Information processing in viruses    03272 Virion - Hepatitis viruses     122910336 (CLDN17)  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04514 Cell adhesion molecules     122910336 (CLDN17)  09140 Cellular Processes   09144 Cellular community - eukaryotes    04530 Tight junction     122910336 (CLDN17)  09150 Organismal Systems   09151 Immune system    04670 Leukocyte transendothelial migration     122910336 (CLDN17)   09158 Development and regeneration    04382 Cornified envelope formation     122910336 (CLDN17)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     122910336 (CLDN17)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:nvs03037]     122910336 (CLDN17)    04147 Exosome [BR:nvs04147]     122910336 (CLDN17) Cilium and associated proteins [BR:nvs03037]  Other cilia and associated proteins   Stereociliary proteins    122910336 (CLDN17) Exosome [BR:nvs04147]  Exosomal proteins   Exosomal proteins of ovarian cancer cells    122910336 (CLDN17)   Exosomal proteins of colorectal cancer cells    122910336 (CLDN17) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PMP22_Claudin Claudin_2 DUF4064 DUF7139 Clc-like Claudin_3 DNER_C Motif Other DBs NCBI-GeneID:  122910336 NCBI-ProteinID:  XP_044110923 UniProt:  A0A8C7ADE4 LinkDB All DBs Position 6:14360081..14360755 Genome browser AA seq 224 aa AA seqDB search MAFYPLQIAGLVLGFLGVVGTLATTLLPQWRVSAFIGSNIIVFERLWEGLWMNCIRQAKV RLQCKFYSSLLALPPVLEAARALMCVAVALSFVALLLGICGMKQVQCTGSNEKAKAYLLG TSGILFILTGIFVLIPVCWTANIIIRDFYNPAIHVGQKRELGAALFLGWASTAILFIAGG LLCGFCCCNRKKQRYRYPAPGYGVPHTEKRRNVTMFSKTSTSYV NT seq 675 nt NT seq  +upstreamnt  +downstreamnt atggcattttatccactgcagattgctggtctggttcttgggttccttggcgtagttggg actcttgccacaacacttctgcctcagtggagggtatcagcttttattggcagcaacatt attgtttttgaaaggctctgggaagggctttggatgaactgcattcgacaagccaaggtc cggttgcagtgcaaattctatagttctttgttggcgctcccacctgtcctagaagcagca cgcgccctcatgtgtgtggcagttgctctctccttcgtcgctctgctccttggcatctgt ggcatgaagcaggtccagtgcacgggctctaacgagaaggccaaagcataccttctaggg acttcggggatcctcttcatcctgaccggcatcttcgttctgattccagtgtgctggaca gccaacatcatcatcagggatttctacaacccagccatccacgtgggtcagaaacgagag ctgggagcagcccttttccttggctgggccagcaccgccatccttttcattgcagggggt ctgctctgtgggttctgctgttgcaacagaaagaagcaaaggtacagatacccagcccct gggtatggtgtgccacacacagagaagcgaaggaacgtgacaatgtttagtaagacttcc accagttatgtctaa

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