Homo sapiens (human): 53842
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
Motif
Other DBs
NCBI-GeneID:
53842
NCBI-ProteinID:
NP_001104789
OMIM:
620566
HGNC:
2044
Ensembl:
ENSG00000177300
UniProt:
Q8N7P3
LinkDB
All DBs
Position
4:complement(183318100..183320276)
Genome browser
AA seq
220 aa
AA seq
DB search
MALVFRTVAQLAGVSLSLLGWVLSCLTNYLPHWKNLNLDLNEMENWTMGLWQTCVIQEEV
GMQCKDFDSFLALPAELRVSRILMFLSNGLGFLGLLVSGFGLDCLRIGESQRDLKRRLLI
LGGILSWASGVTALVPVSWVAHKTVQEFWDENVPDFVPRWEFGEALFLGWFAGLSLLLGG
CLLHCAACSSHAPLASGHYAVAQTQDHHQELETRNTNLKH
NT seq
663 nt
NT seq
+upstream
nt +downstream
nt
atggctttagtatttagaactgtagctcaactagctggagtttcattatctttgctggga
tgggttttatcctgtcttacaaactacctgccacactggaagaacctcaacctggactta
aatgaaatggaaaactggaccatgggactctggcaaacctgtgtcatccaagaggaagtg
gggatgcaatgcaaggactttgactccttcctggctttgcctgctgaactcagggtctcc
aggatcttaatgtttctgtcaaatgggctgggatttctgggcctgctggtctctgggttt
ggcctggactgtttgagaattggagagagtcagagagatctcaagaggcgactgctgatc
ctgggaggaattctgtcctgggcctcgggagtcacagccctggttcccgtctcttgggtt
gcccacaagacggttcaggagttctgggatgagaacgtcccagactttgtccccaggtgg
gagtttggggaggccctgtttctgggctggtttgctggactttctcttctgctaggaggg
tgtctgctccactgtgcagcctgctccagccacgctcccctagcttcgggccactacgca
gtggcacaaacacaagatcatcatcaagaactggagacgagaaacaccaacctgaaacac
taa
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