KEGG   Homo sapiens (human): 9080
Entry
9080              CDS       T01001                                 
Symbol
CLDN9, DFNB116
Name
(RefSeq) claudin 9
  KO
K06087  claudin
Organism
hsa  Homo sapiens (human)
Pathway
hsa03272  Virion - Hepatitis viruses
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
Disease
H00605  Deafness, autosomal recessive
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09125 Information processing in viruses
   03272 Virion - Hepatitis viruses
    9080 (CLDN9)
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    9080 (CLDN9)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04530 Tight junction
    9080 (CLDN9)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    9080 (CLDN9)
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    9080 (CLDN9)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    9080 (CLDN9)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    9080 (CLDN9)
   04147 Exosome [BR:hsa04147]
    9080 (CLDN9)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   9080 (CLDN9)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of ovarian cancer cells
   9080 (CLDN9)
  Exosomal proteins of colorectal cancer cells
   9080 (CLDN9)
SSDB
Motif
Pfam: PMP22_Claudin Claudin_2 TMEM_230_134 DUF7139
Other DBs
NCBI-GeneID: 9080
NCBI-ProteinID: NP_066192
OMIM: 615799
HGNC: 2051
Ensembl: ENSG00000213937
UniProt: O95484
Structure
LinkDB
Position
16:3012923..3014505
AA seq 217 aa
MASTGLELLGMTLAVLGWLGTLVSCALPLWKVTAFIGNSIVVAQVVWEGLWMSCVVQSTG
QMQCKVYDSLLALPQDLQAARALCVIALLLALLGLLVAITGAQCTTCVEDEGAKARIVLT
AGVILLLAGILVLIPVCWTAHAIIQDFYNPLVAEALKRELGASLYLGWAAAALLMLGGGL
LCCTCPPPQVERPRGPRLGYSIPSRSGASGLDKRDYV
NT seq 654 nt   +upstreamnt  +downstreamnt
atggcttcgaccggcttagaactgctgggcatgaccctggctgtgctgggctggctgggg
accctggtgtcctgcgccctgcccctgtggaaggtgaccgccttcatcggcaacagcatc
gtggtggcccaggtggtgtgggagggcctgtggatgtcctgcgtggtgcagagcacgggc
cagatgcagtgcaaggtgtacgactcactgctggctctgccgcaggacctgcaggccgca
cgtgccctctgtgtcattgccctcctgctggccctgcttggcctcctggtggccatcaca
ggtgcccagtgtaccacgtgtgtggaggacgaaggtgccaaggcccgtatcgtgctcacc
gcgggggtcatcctcctcctcgccggcatcctggtgctcatccctgtgtgctggacggcg
cacgccatcatccaggacttctacaaccccctggtggctgaggccctcaagcgggagctg
ggggcctccctctacctgggctgggcggcggctgcactgcttatgctgggcggggggctc
ctctgctgcacgtgccccccgccccaggtcgagcggccccgcggacctcggctgggctac
tccatcccctcccgctcgggtgcatctggactggacaagagggactacgtgtga

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