Neogale vison (American mink): 122913973
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Entry
122913973 CDS
T08764
Symbol
CLDN25
Name
(RefSeq) putative claudin-25
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
122913973 (CLDN25)
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecules
122913973 (CLDN25)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04530 Tight junction
122913973 (CLDN25)
09150 Organismal Systems
09151 Immune system
04670 Leukocyte transendothelial migration
122913973 (CLDN25)
09158 Development and regeneration
04382 Cornified envelope formation
122913973 (CLDN25)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
122913973 (CLDN25)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
nvs03037
]
122913973 (CLDN25)
04147 Exosome [BR:
nvs04147
]
122913973 (CLDN25)
Cilium and associated proteins [BR:
nvs03037
]
Other cilia and associated proteins
Stereociliary proteins
122913973 (CLDN25)
Exosome [BR:
nvs04147
]
Exosomal proteins
Exosomal proteins of ovarian cancer cells
122913973 (CLDN25)
Exosomal proteins of colorectal cancer cells
122913973 (CLDN25)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
Motif
Other DBs
NCBI-GeneID:
122913973
NCBI-ProteinID:
XP_044116553
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All DBs
Position
7:104146263..104146949
Genome browser
AA seq
228 aa
AA seq
DB search
MAWSLRGKAQLGGLLLSLLGWVCSCVTTILPQWKTLSLDLNEMEIWVMGLWEVCVNQEEV
AVCKAFESFLSLPQELQVSRILMAASHGLGLLGLLLSGFGSECFQLHRIRWVFKRRLCLL
GGTLETSAAATTLLPVSWVAYATVQDFWDNSIPEIVPRWEFGDALYLGWAAGIFLALGGL
VLIFSACLGKEDVPSLQMAGPTAPPFYAPEDESSDSFYLTPRPRNVFI
NT seq
687 nt
NT seq
+upstream
nt +downstream
nt
atggcctggagtctccgcgggaaagcccagcttggaggactgctcctctctctcctcggc
tgggtctgctcctgtgtcaccaccatcctaccgcagtggaagactctcagtctggacctg
aacgaaatggagatctgggtcatgggactttgggaggtctgcgtgaatcaggaggaagtt
gccgtgtgcaaggcctttgagtccttcttgtctctgccccaggaactccaggtatcccgc
atcctgatggcagcctcccacgggctggggctactggggcttctgctctctggctttggg
tccgaatgcttccagttgcacaggatcagatgggtatttaaaagacggctttgtctcctg
ggagggactctggaaacatcagctgcagccactaccctcctcccagtctcttgggtggcc
tacgccaccgtccaagacttctgggataatagcatccctgagattgtgcctcgctgggag
tttggagatgccctctacctgggctgggctgctgggattttcctggccctcggtgggtta
gtcctcatcttttcagcgtgtctgggaaaagaagatgtgccctccctccagatggctggc
cctacagccccaccattctatgccccagaggatgagtccagtgactccttctatctaaca
ccaagacccaggaacgtattcatctag
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