Mustela nigripes (black-footed ferret): 132026987
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Entry
132026987 CDS
T09425
Symbol
CLDN6
Name
(RefSeq) claudin-6
KO
K06087
claudin
Organism
mnp
Mustela nigripes (black-footed ferret)
Pathway
mnp03272
Virion - Hepatitis viruses
mnp04382
Cornified envelope formation
mnp04514
Cell adhesion molecule (CAM) interaction
mnp04530
Tight junction
mnp04670
Leukocyte transendothelial migration
mnp05160
Hepatitis C
Brite
KEGG Orthology (KO) [BR:
mnp00001
]
09120 Genetic Information Processing
09125 Information processing in viruses
03272 Virion - Hepatitis viruses
132026987 (CLDN6)
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecule (CAM) interaction
132026987 (CLDN6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04530 Tight junction
132026987 (CLDN6)
09150 Organismal Systems
09151 Immune system
04670 Leukocyte transendothelial migration
132026987 (CLDN6)
09158 Development and regeneration
04382 Cornified envelope formation
132026987 (CLDN6)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
132026987 (CLDN6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
mnp03037
]
132026987 (CLDN6)
04147 Exosome [BR:
mnp04147
]
132026987 (CLDN6)
Cilium and associated proteins [BR:
mnp03037
]
Other cilia and associated proteins
Stereociliary proteins
132026987 (CLDN6)
Exosome [BR:
mnp04147
]
Exosomal proteins
Exosomal proteins of ovarian cancer cells
132026987 (CLDN6)
Exosomal proteins of colorectal cancer cells
132026987 (CLDN6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
Motif
Other DBs
NCBI-GeneID:
132026987
NCBI-ProteinID:
XP_059271542
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All DBs
Position
11:36897258..36900083
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AA seq
221 aa
AA seq
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MASAGLQILGIVLTLLGWVNGLVSCALPLWKVTAFIGNSIVVAQVVWEGLWMSCVVQSTG
QMQCKVYDSLLALPQDLQAARALCVVALLVALLGLLVYLAGAKCTTCVEDKDSKARLVLV
SGIIFVISGVLILIPVCWTAHAIIRDFYNPLVSDAQKRELGASLYLGWAASGLLLLGGGL
LCCTCPSGRSRGPNHYMARYSASAAQATSQGAPEYPTKNYV
NT seq
666 nt
NT seq
+upstream
nt +downstream
nt
atggcttctgctggtctgcaaatcctggggattgtcctgacactgcttggctgggtaaat
ggtctggtgtcgtgtgccctgcccctgtggaaggtgaccgccttcatcggcaacagcatc
gtggtggcccaggtggtatgggagggtctgtggatgtcctgcgtggtgcagagcaccggc
cagatgcagtgcaaggtctacgactccctgctggcgctgccccaggacctgcaggctgct
cgcgccctctgcgtcgttgccctccttgtggccctgctcgggctgctggtctacctcgcg
ggagccaagtgtaccacctgcgtggaggacaaggactccaaggcccgtctggtgctagtc
tctgggatcatctttgtcatctcaggggtcctgatcctgatccccgtatgctggacggct
catgccatcatccgggacttctacaaccccctggtgtcagacgcccaaaagcgggagctg
ggggcctctctctacttgggctgggcagcctccggccttttgttgttgggcggggggctg
ctgtgctgcacctgtccctctgggaggtcccggggcccaaaccattatatggcccgctac
tcggcatcagccgcacaggccacctctcagggtgcccctgagtaccccactaagaattac
gtctaa
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