KEGG   Homo sapiens (human): 24146
Entry
24146             CDS       T01001                                 
Symbol
CLDN15
Name
(RefSeq) claudin 15
  KO
K06087  claudin
Organism
hsa  Homo sapiens (human)
Pathway
hsa04514  Cell adhesion molecules
hsa04530  Tight junction
hsa04670  Leukocyte transendothelial migration
hsa05130  Pathogenic Escherichia coli infection
hsa05160  Hepatitis C
Network
nt06180  Pathogenic Escherichia coli
  Element
N01287  Tight junction-Actin signaling pathway
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    24146 (CLDN15)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04530 Tight junction
    24146 (CLDN15)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    24146 (CLDN15)
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    24146 (CLDN15)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    24146 (CLDN15)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    24146 (CLDN15)
   04147 Exosome [BR:hsa04147]
    24146 (CLDN15)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   24146 (CLDN15)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of ovarian cancer cells
   24146 (CLDN15)
  Exosomal proteins of colorectal cancer cells
   24146 (CLDN15)
SSDB
Motif
Pfam: PMP22_Claudin Claudin_2
Other DBs
NCBI-GeneID: 24146
NCBI-ProteinID: NP_001172009
OMIM: 615778
HGNC: 2036
Ensembl: ENSG00000106404
UniProt: P56746
Position
7:complement(101232094..101238820)
AA seq 228 aa
MSMAVETFGFFMATVGLLMLGVTLPNSYWRVSTVHGNVITTNTIFENLWFSCATDSLGVY
NCWEFPSMLALSGYIQACRALMITAILLGFLGLLLGIAGLRCTNIGGLELSRKAKLAATA
GALHILAGICGMVAISWYAFNITRDFFDPLYPGTKYELGPALYLGWSASLISILGGLCLC
SACCCGSDEDPAASARRPYQAPVSVMPVATSDQEGDSSFGKYGRNAYV
NT seq 687 nt   +upstreamnt  +downstreamnt
atgtcgatggctgtggaaacctttggcttcttcatggcaactgtggggctgctgatgctg
ggggtgactctgccaaacagctactggcgagtgtccactgtgcacgggaacgtcatcacc
accaacaccatcttcgagaacctctggtttagctgtgccaccgactccctgggcgtctac
aactgctgggagttcccgtccatgctggccctctctgggtatattcaggcctgccgggca
ctcatgatcaccgccatcctcctgggcttcctcggcctcttgctaggcatagcgggcctg
cgctgcaccaacattgggggcctggagctctccaggaaagccaagctggcggccaccgca
ggggccctccacattctggccggtatctgcgggatggtggccatctcctggtacgccttc
aacatcacccgggacttcttcgaccccttgtaccccggaaccaagtacgagctgggcccc
gccctctacctggggtggagcgcctcactgatctccatcctgggtggcctctgcctctgc
tccgcctgctgctgcggctctgacgaggacccagccgccagcgcccggcggccctaccag
gctccagtgtccgtgatgcccgtcgccacctcggaccaagaaggcgacagcagctttggc
aaatacggcagaaacgcctacgtgtag

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