KEGG   Homo sapiens (human): 10686
Entry
10686             CDS       T01001                                 
Symbol
CLDN16, HOMG3, PCLN1
Name
(RefSeq) claudin 16
  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
Disease
H01210  Hypomagnesemia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09125 Information processing in viruses
   03272 Virion - Hepatitis viruses
    10686 (CLDN16)
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    10686 (CLDN16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04530 Tight junction
    10686 (CLDN16)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    10686 (CLDN16)
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    10686 (CLDN16)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    10686 (CLDN16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    10686 (CLDN16)
   04147 Exosome [BR:hsa04147]
    10686 (CLDN16)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   10686 (CLDN16)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of ovarian cancer cells
   10686 (CLDN16)
  Exosomal proteins of colorectal cancer cells
   10686 (CLDN16)
SSDB
Motif
Pfam: PMP22_Claudin Claudin_2 Clc-like aGPT-Pplase3 DuoxA
Other DBs
NCBI-GeneID: 10686
NCBI-ProteinID: NP_006571
OMIM: 603959
HGNC: 2037
Ensembl: ENSG00000113946
Pharos: Q9Y5I7(Tbio)
UniProt: Q9Y5I7
Position
3:190290361..190412138
AA seq 235 aa
MRDLLQYIACFFAFFSAGFLIVATWTDCWMVNADDSLEVSTKCRGLWWECVTNAFDGIRT
CDEYDSILAEHPLKLVVTRALMITADILAGFGFLTLLLGLDCVKFLPDEPYIKVRICFVA
GATLLIAGTPGIIGSVWYAVDVYVERSTLVLHNIFLGIQYKFGWSCWLGMAGSLGCFLAG
AVLTCCLYLFKDVGPERNYPYSLRKAYSAAGVSMAKSYSAPRTETAKMYAVDTRV
NT seq 708 nt   +upstreamnt  +downstreamnt
atgagggatcttcttcaatacatcgcttgcttctttgcctttttctctgctgggtttttg
attgtggccacctggactgactgttggatggtgaatgctgatgactctctggaggtgagc
acaaaatgccgaggcctctggtgggaatgcgtcacaaatgcttttgatgggattcgcacc
tgtgatgagtacgattccatacttgcggagcatcccttgaagctggtggtaactcgagcg
ttgatgattactgcagatattctagctgggtttggatttctcaccctgctccttggtctt
gactgcgtgaaattcctccctgatgagccgtacattaaagtccgcatctgctttgttgct
ggagccacgttactaatagcaggtaccccaggaatcattggctctgtgtggtatgctgtt
gatgtgtatgtggaacgttctactttggttttgcacaatatatttcttggtatccaatat
aaatttggttggtcctgttggctcggaatggctgggtctctgggttgctttttggctgga
gctgttctcacctgctgcttatatctttttaaagatgttggacctgagagaaactatcct
tattccttgaggaaagcctattcagccgcgggtgtttccatggccaagtcatactcagcc
cctcgcacagagacggccaaaatgtatgctgtagacacaagggtgtaa

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