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
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
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09125 Information processing in viruses
   03272 Virion - Hepatitis viruses
    137075 (CLDN23)
 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 Yip1 TMEM_230_134 DUF2970 Clc-like
Other DBs
NCBI-GeneID: 137075
NCBI-ProteinID: NP_919260
OMIM: 609203
HGNC: 17591
Ensembl: ENSG00000253958
UniProt: Q96B33
LinkDB
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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