KEGG   Homo sapiens (human): 149461
Entry
149461            CDS       T01001                                 
Symbol
CLDN19, HOMG5
Name
(RefSeq) claudin 19
  KO
K06087  claudin
Organism
hsa  Homo sapiens (human)
Pathway
hsa03272  Virion - Hepatitis viruses
hsa04382  Cornified envelope formation
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
    149461 (CLDN19)
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04514 Cell adhesion molecules
    149461 (CLDN19)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04530 Tight junction
    149461 (CLDN19)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    149461 (CLDN19)
  09158 Development and regeneration
   04382 Cornified envelope formation
    149461 (CLDN19)
 09160 Human Diseases
  09172 Infectious disease: viral
   05160 Hepatitis C
    149461 (CLDN19)
  09171 Infectious disease: bacterial
   05130 Pathogenic Escherichia coli infection
    149461 (CLDN19)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    149461 (CLDN19)
   04147 Exosome [BR:hsa04147]
    149461 (CLDN19)
Cilium and associated proteins [BR:hsa03037]
 Other cilia and associated proteins
  Stereociliary proteins
   149461 (CLDN19)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of ovarian cancer cells
   149461 (CLDN19)
  Exosomal proteins of colorectal cancer cells
   149461 (CLDN19)
SSDB
Motif
Pfam: PMP22_Claudin Claudin_2 Mntp Amastin TMEM127 SUR7
Other DBs
NCBI-GeneID: 149461
NCBI-ProteinID: NP_683763
OMIM: 610036
HGNC: 2040
Ensembl: ENSG00000164007
UniProt: Q8N6F1
LinkDB
Position
1:complement(42733093..42740236)
AA seq 224 aa
MANSGLQLLGYFLALGGWVGIIASTALPQWKQSSYAGDAIITAVGLYEGLWMSCASQSTG
QVQCKLYDSLLALDGHIQSARALMVVAVLLGFVAMVLSVVGMKCTRVGDSNPIAKGRVAI
AGGALFILAGLCTLTAVSWYATLVTQEFFNPSTPVNARYEFGPALFVGWASAGLAVLGGS
FLCCTCPEPERPNSSPQPYRPGPSAAAREPVVKLPASAKGPLGV
NT seq 675 nt   +upstreamnt  +downstreamnt
atggccaactcaggcctccagctcctgggctacttcttggccctgggtggctgggtgggc
atcattgctagcacagccctgccacagtggaagcagtcttcctacgcaggcgacgccatc
atcactgccgtgggcctctatgaagggctctggatgtcctgcgcctcccagagcactggg
caagtgcagtgcaagctctacgactcgctgctcgccctggacggtcacatccaatcagcg
cgggccctgatggtggtggccgtgctcctgggcttcgtggccatggtcctcagcgtagtt
ggcatgaagtgtacgcgggtgggagacagcaaccccattgccaagggccgtgttgccatc
gccgggggagccctcttcatcctggcaggcctctgcactttgactgctgtctcgtggtat
gccaccctggtgacccaggagttcttcaacccaagcacacctgtcaatgccaggtatgaa
tttggcccagccctgttcgtgggctgggcctcagctggcctggccgtgctgggcggctcc
ttcctctgctgcacatgcccggagccagagagacccaacagcagcccacagccctatcgg
cctggaccctctgctgctgcccgagaaccagttgttaaattgcccgcctccgccaagggc
cccctgggtgtgtaa

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