Macaca mulatta (rhesus monkey): 701348
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Entry
701348 CDS
T01028
Symbol
CLDN22
Name
(RefSeq) claudin-22
KO
K06087
claudin
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc03272
Virion - Hepatitis viruses
mcc04382
Cornified envelope formation
mcc04514
Cell adhesion molecules
mcc04530
Tight junction
mcc04670
Leukocyte transendothelial migration
mcc05160
Hepatitis C
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09120 Genetic Information Processing
09125 Information processing in viruses
03272 Virion - Hepatitis viruses
701348 (CLDN22)
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecules
701348 (CLDN22)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04530 Tight junction
701348 (CLDN22)
09150 Organismal Systems
09151 Immune system
04670 Leukocyte transendothelial migration
701348 (CLDN22)
09158 Development and regeneration
04382 Cornified envelope formation
701348 (CLDN22)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
701348 (CLDN22)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
mcc03037
]
701348 (CLDN22)
04147 Exosome [BR:
mcc04147
]
701348 (CLDN22)
Cilium and associated proteins [BR:
mcc03037
]
Other cilia and associated proteins
Stereociliary proteins
701348 (CLDN22)
Exosome [BR:
mcc04147
]
Exosomal proteins
Exosomal proteins of ovarian cancer cells
701348 (CLDN22)
Exosomal proteins of colorectal cancer cells
701348 (CLDN22)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
Motif
Other DBs
NCBI-GeneID:
701348
NCBI-ProteinID:
NP_001252773
Ensembl:
ENSMMUG00000030008
UniProt:
F6S639
A0A8J8XTZ7
LinkDB
All DBs
Position
5:complement(180630270..180631899)
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AA seq
219 aa
AA seq
DB search
MALVFRTVAQLAGVSLSLLGWVLSCLTNYLPHWKNLNLDLNEMENWTMGLWQTCVTQEEV
GMQCKDFDSFLALPAELRVSRILMFLSNGLGFLGLLVSGFGLDCLRIGEGQRDLKRRLLI
LGGVLSWASGITALVPVSWVAHKTVQEFWDENVPDFVPRWEFGEALFLGWFAGLSLLLGG
CLLNCAACSSHALLASGHHAVAQMQDHHQLETRNTNLKN
NT seq
660 nt
NT seq
+upstream
nt +downstream
nt
atggctttagtatttagaactgtggctcaactagctggagtttcattatctttgctggga
tgggttttatcctgtcttacaaactacctgccacactggaagaacctcaacctggactta
aatgaaatggaaaactggaccatgggactctggcaaacctgcgtcacccaagaggaagtg
ggaatgcaatgcaaggactttgactccttcctggctttgcctgctgaactcagggtctcc
aggatcttaatgtttctatcaaacgggctgggatttctgggcctgctggtctctgggttt
ggcctggactgtttgagaattggagagggtcagagagatctcaagaggcgactgctgatc
ctgggaggagttctgtcctgggcctcgggaatcacagccctggttcctgtctcttgggtt
gcccacaagacggttcaggagttctgggatgagaacgtcccagactttgtccccaggtgg
gagtttggggaggccctctttctgggctggtttgctggactttctcttctactgggaggg
tgtctgctcaactgtgcagcctgttccagccacgctctcctagcttcgggccaccatgca
gtggcgcaaatgcaagatcatcatcaactggagacaagaaacaccaacctgaaaaactaa
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