Galeopterus variegatus (Sunda flying lemur): 103585358
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Entry
103585358 CDS
T08727
Symbol
CLDN6
Name
(RefSeq) claudin-6
KO
K06087
claudin
Organism
gvr
Galeopterus variegatus (Sunda flying lemur)
Pathway
gvr03272
Virion - Hepatitis viruses
gvr04382
Cornified envelope formation
gvr04514
Cell adhesion molecule (CAM) interaction
gvr04530
Tight junction
gvr04670
Leukocyte transendothelial migration
gvr05160
Hepatitis C
Brite
KEGG Orthology (KO) [BR:
gvr00001
]
09120 Genetic Information Processing
09125 Information processing in viruses
03272 Virion - Hepatitis viruses
103585358 (CLDN6)
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecule (CAM) interaction
103585358 (CLDN6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04530 Tight junction
103585358 (CLDN6)
09150 Organismal Systems
09151 Immune system
04670 Leukocyte transendothelial migration
103585358 (CLDN6)
09158 Development and regeneration
04382 Cornified envelope formation
103585358 (CLDN6)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
103585358 (CLDN6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
gvr03037
]
103585358 (CLDN6)
04147 Exosome [BR:
gvr04147
]
103585358 (CLDN6)
Cilium and associated proteins [BR:
gvr03037
]
Other cilia and associated proteins
Stereociliary proteins
103585358 (CLDN6)
Exosome [BR:
gvr04147
]
Exosomal proteins
Exosomal proteins of ovarian cancer cells
103585358 (CLDN6)
Exosomal proteins of colorectal cancer cells
103585358 (CLDN6)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
Motif
Other DBs
NCBI-GeneID:
103585358
NCBI-ProteinID:
XP_008564508
UniProt:
A0ABM0Q817
LinkDB
All DBs
Position
Unknown
AA seq
221 aa
AA seq
DB search
MASAGLQILGIILTLLGWVNALVSCTLPMWKVTAFIGNSIVVAQVVWEGLWMSCVVQSTG
QMQCKVYDSLLALPQDLQAARALCVITLLVALLGLLVYLAGAKCTTCVEDKDSKARLVLT
SGIIFLISGVLTLIPICWTANAIIQDFYNPLVAEAQKRELGASLYLGWAASGLLLLGGGL
LCCTCPSGGSRGSSNYMARYSVSVPHTTSRGPSEYPTKNYV
NT seq
666 nt
NT seq
+upstream
nt +downstream
nt
atggcctctgctggtctgcaaatcctgggaatcatcctgacactgctgggctgggtgaat
gccctggtgtcctgcaccctgcccatgtggaaggtgactgccttcatcggcaacagcatc
gtggtggcccaggtggtgtgggagggcctgtggatgtcctgcgtggtgcagagcaccggc
cagatgcagtgcaaggtgtacgactctctgctggccctgccccaggacctgcaggctgca
cgtgccctctgtgtcatcaccctccttgtggccctgctcggcctgctggtctaccttgct
ggagccaagtgtaccacctgtgtggaggacaaggactctaaggcccgcctggtgctcacc
tctggaatcatcttcctcatatcaggagtcctgaccctgatccccatctgctggactgcc
aatgccatcatccaggacttctacaaccccctggtggctgaagcccaaaagcgggagcta
ggggcctccctctacctgggctgggcagcctcgggccttttgttgctgggcggggggctg
ctgtgctgcacctgtccttctgggggttcccgaggctccagcaattacatggcccgctac
tcagtatctgtcccgcataccacctctcgggggccctctgagtacccaaccaagaattat
gtgtga
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