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
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
    100132463 (CLDN24)
 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
LinkDB
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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