Neogale vison (American mink): 122910481
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Entry
122910481 CDS
T08764
Symbol
CLDN11
Name
(RefSeq) claudin-11
KO
K06087
claudin
Organism
nvs
Neogale vison (American mink)
Pathway
nvs03272
Virion - Hepatitis viruses
nvs04382
Cornified envelope formation
nvs04514
Cell adhesion molecules
nvs04530
Tight junction
nvs04670
Leukocyte transendothelial migration
nvs05160
Hepatitis C
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09120 Genetic Information Processing
09125 Information processing in viruses
03272 Virion - Hepatitis viruses
122910481 (CLDN11)
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecules
122910481 (CLDN11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04530 Tight junction
122910481 (CLDN11)
09150 Organismal Systems
09151 Immune system
04670 Leukocyte transendothelial migration
122910481 (CLDN11)
09158 Development and regeneration
04382 Cornified envelope formation
122910481 (CLDN11)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
122910481 (CLDN11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
nvs03037
]
122910481 (CLDN11)
04147 Exosome [BR:
nvs04147
]
122910481 (CLDN11)
Cilium and associated proteins [BR:
nvs03037
]
Other cilia and associated proteins
Stereociliary proteins
122910481 (CLDN11)
Exosome [BR:
nvs04147
]
Exosomal proteins
Exosomal proteins of ovarian cancer cells
122910481 (CLDN11)
Exosomal proteins of colorectal cancer cells
122910481 (CLDN11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
zf-LITAF-like
Motif
Other DBs
NCBI-GeneID:
122910481
NCBI-ProteinID:
XP_044111043
LinkDB
All DBs
Position
6:94651417..94667418
Genome browser
AA seq
207 aa
AA seq
DB search
MVATCLQVVGFVTSFVGWIGIIVTTSTNDWVVTCGYTIPTCRKLDELGSKGLWADCVMAT
GLYHCKPLVDILILPGYVQACRALMIAASVLGLPAILLLLTVLPCIRMGHEPGVAKYRRA
QLAGVLLILLALCAIVATIWFPVCAHRETTIVSFGYSLYAGWIGAVLCLVGGCVIVCCAG
DAQSFGENRFYYSSGSSSPTHAKSAHV
NT seq
624 nt
NT seq
+upstream
nt +downstream
nt
atggtggccacgtgcctgcaggtagtgggcttcgtcacgagcttcgtgggttggatcggc
atcatcgtcaccacgtccactaatgactgggtggtgacctgcggctacaccatccccacc
tgccgcaagctggacgaactgggctccaaggggctgtgggccgactgcgtcatggccacg
gggctgtaccactgcaagcccctggtggacatcctcatcctgccgggctatgtccaggcc
tgccgagccctgatgattgcagcctcagtcctggggctgcccgccattctcctgctgctg
acggttctcccctgcattcgaatgggccatgagcccggtgtggccaagtacaggcgggct
cagctggctggtgtgctgctcattctgctggctctctgtgccatcgttgccaccatctgg
ttccccgtgtgcgcccaccgtgagaccaccatcgtgagctttggctactccctgtacgcg
ggctggatcggggctgtgctgtgcctcgtgggtggctgtgtcatcgtctgctgcgctgga
gatgcccagtcgtttggtgaaaaccgcttctactactcttcgggctccagctccccgact
catgccaagagtgcccacgtataa
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