KEGG   Homo sapiens (human): 137075
Entry
137075            CDS       T01001                                 
Symbol
CLDN23, CLDNL, hCG1646163
Name
(RefSeq) claudin 23
  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
    137075 (CLDN23)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04530 Tight junction
    137075 (CLDN23)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    137075 (CLDN23)
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    137075 (CLDN23)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    137075 (CLDN23)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    137075 (CLDN23)
   04147 Exosome [BR:hsa04147]
    137075 (CLDN23)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   137075 (CLDN23)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of ovarian cancer cells
   137075 (CLDN23)
  Exosomal proteins of colorectal cancer cells
   137075 (CLDN23)
SSDB
Motif
Pfam: PMP22_Claudin Claudin_2 TMEM_230_134 Clc-like
Other DBs
NCBI-GeneID: 137075
NCBI-ProteinID: NP_919260
OMIM: 609203
HGNC: 17591
Ensembl: ENSG00000253958
UniProt: Q96B33
Position
8:8701937..8704096
AA seq 292 aa
MRTPVVMTLGMVLAPCGLLLNLTGTLAPGWRLVKGFLNQPVDVELYQGLWDMCREQSSRE
RECGQTDQWGYFEAQPVLVARALMVTSLAATVLGLLLASLGVRCWQDEPNFVLAGLSGVV
LFVAGLLGLIPVSWYNHFLGDRDVLPAPASPVTVQVSYSLVLGYLGSCLLLLGGFSLALS
FAPWCDERCRRRRKGPSAGPRRSSVSTIQVEWPEPDLAPAIKYYSDGQHRPPPAQHRKPK
PKPKVGFPMPRPRPKAYTNSVDVLDGEGWESQDAPSCSTHPCDSSLPCDSDL
NT seq 879 nt   +upstreamnt  +downstreamnt
atgcggacgccggtggtgatgacgctgggcatggtgttggcgccctgcgggctcctgctc
aacctgaccggcaccctggcgcccggctggcggctggtgaagggcttcctgaaccagcca
gtggacgtggagttgtaccagggcctgtgggacatgtgtcgcgagcagagcagccgcgag
cgcgagtgcggccagacggaccagtggggctacttcgaggcccagcccgtgctggtggcg
cgggcactcatggtcacctcgctggccgccacggtcctggggcttctgctggcgtcgctg
ggcgtgcgctgctggcaggacgagcccaacttcgtgctggcagggctctcgggcgtcgtg
ctcttcgtcgctggcctcctcggcctcatcccggtgtcctggtacaaccacttcttgggg
gaccgcgacgtgctgcccgccccggccagcccggtcacggtgcaggtcagctacagcctg
gtcctgggctacctgggcagctgcctcctgctgctgggcggcttctcgctggcgctcagc
ttcgcgccctggtgcgacgagcgttgtcgccgccgccgcaagggaccctccgccgggcct
cgccgcagcagcgtcagcaccatccaagtggagtggcccgagcccgacctggcgcccgcc
atcaagtactacagcgacggccagcaccgaccgccgcctgcccagcaccgcaagcccaag
cccaagcccaaggtcggcttccccatgccgcggccgcggcccaaggcctacaccaactcg
gtggacgtcctcgacggggaggggtgggagtcccaggacgctccctcgtgcagcacccac
ccctgcgacagctcgctgccctgcgactccgacctctag

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