KEGG   Homo sapiens (human): 53842
Entry
53842             CDS       T01001                                 
Symbol
CLDN22, CLDN21
Name
(RefSeq) claudin 22
  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
    53842 (CLDN22)
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    53842 (CLDN22)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04530 Tight junction
    53842 (CLDN22)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    53842 (CLDN22)
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    53842 (CLDN22)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    53842 (CLDN22)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    53842 (CLDN22)
   04147 Exosome [BR:hsa04147]
    53842 (CLDN22)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   53842 (CLDN22)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of ovarian cancer cells
   53842 (CLDN22)
  Exosomal proteins of colorectal cancer cells
   53842 (CLDN22)
SSDB
Motif
Pfam: PMP22_Claudin Claudin_2
Other DBs
NCBI-GeneID: 53842
NCBI-ProteinID: NP_001104789
OMIM: 620566
HGNC: 2044
Ensembl: ENSG00000177300
UniProt: Q8N7P3
LinkDB
Position
4:complement(183318100..183320276)
AA seq 220 aa
MALVFRTVAQLAGVSLSLLGWVLSCLTNYLPHWKNLNLDLNEMENWTMGLWQTCVIQEEV
GMQCKDFDSFLALPAELRVSRILMFLSNGLGFLGLLVSGFGLDCLRIGESQRDLKRRLLI
LGGILSWASGVTALVPVSWVAHKTVQEFWDENVPDFVPRWEFGEALFLGWFAGLSLLLGG
CLLHCAACSSHAPLASGHYAVAQTQDHHQELETRNTNLKH
NT seq 663 nt   +upstreamnt  +downstreamnt
atggctttagtatttagaactgtagctcaactagctggagtttcattatctttgctggga
tgggttttatcctgtcttacaaactacctgccacactggaagaacctcaacctggactta
aatgaaatggaaaactggaccatgggactctggcaaacctgtgtcatccaagaggaagtg
gggatgcaatgcaaggactttgactccttcctggctttgcctgctgaactcagggtctcc
aggatcttaatgtttctgtcaaatgggctgggatttctgggcctgctggtctctgggttt
ggcctggactgtttgagaattggagagagtcagagagatctcaagaggcgactgctgatc
ctgggaggaattctgtcctgggcctcgggagtcacagccctggttcccgtctcttgggtt
gcccacaagacggttcaggagttctgggatgagaacgtcccagactttgtccccaggtgg
gagtttggggaggccctgtttctgggctggtttgctggactttctcttctgctaggaggg
tgtctgctccactgtgcagcctgctccagccacgctcccctagcttcgggccactacgca
gtggcacaaacacaagatcatcatcaagaactggagacgagaaacaccaacctgaaacac
taa

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