KEGG   Homo sapiens (human): 100132463
Entry
100132463         CDS       T01001                                 
Symbol
CLDN24, CLDN21
Name
(RefSeq) claudin 24
  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
    100132463 (CLDN24)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04530 Tight junction
    100132463 (CLDN24)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    100132463 (CLDN24)
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    100132463 (CLDN24)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    100132463 (CLDN24)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    100132463 (CLDN24)
   04147 Exosome [BR:hsa04147]
    100132463 (CLDN24)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   100132463 (CLDN24)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of ovarian cancer cells
   100132463 (CLDN24)
  Exosomal proteins of colorectal cancer cells
   100132463 (CLDN24)
SSDB
Motif
Pfam: PMP22_Claudin Claudin_2 Clc-like
Other DBs
NCBI-GeneID: 100132463
NCBI-ProteinID: NP_001172078
HGNC: 37200
Ensembl: ENSG00000185758
UniProt: A6NM45
Position
4:complement(183321764..183322426)
AA seq 220 aa
MALIFRTAMQSVGLLLSLLGWILSIITTYLPHWKNLNLDLNEMENWTMGLWQTCVIQEEV
GMQCKDFDSFLALPAELRVSRILMFLSNGLGFLGLLVSGFGLDCLRIGESQRDLKRRLLI
LGGILSWASGITALVPVSWVAHKTVQEFWDENVPDFVPRWEFGEALFLGWFAGLSLLLGG
CLLNCAACSSHAPLALGHYAVAQMQTQCPYLEDGTADPQV
NT seq 663 nt   +upstreamnt  +downstreamnt
atggctttaatctttagaacagcaatgcaatctgttggacttttactatctctcctggga
tggattttatccattattacaacttatttgccacactggaagaacctcaacctggactta
aatgaaatggaaaactggaccatgggactctggcaaacctgtgtcatccaagaggaagtg
gggatgcaatgcaaggactttgactccttcctggctttgcctgctgaactcagggtctcc
aggatcttaatgtttctgtcaaatgggctgggatttctgggcctgctggtctctgggttt
ggcctggactgtttgagaattggagagagtcagagagatctcaagaggcgactgctcatt
ctgggaggaattctgtcctgggcctcgggaatcacagccctggttcccgtctcttgggtt
gcccacaagacggttcaggagttctgggatgagaacgtcccagactttgtccccaggtgg
gagtttggggaggccctgtttctgggctggtttgctggactttctcttctgctaggaggg
tgtctgctcaactgcgcagcctgctccagccacgctcccctagctttgggccactatgca
gtggcgcaaatgcaaactcagtgtccctacctggaagatgggacagcagatcctcaagtg
taa

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