Pan paniscus (bonobo): 100978259
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Entry
100978259 CDS
T02283
Symbol
CLDN10
Name
(RefSeq) claudin-10 isoform X2
KO
K06087
claudin
Organism
pps
Pan paniscus (bonobo)
Pathway
pps03272
Virion - Hepatitis viruses
pps04382
Cornified envelope formation
pps04514
Cell adhesion molecule (CAM) interaction
pps04530
Tight junction
pps04670
Leukocyte transendothelial migration
pps05160
Hepatitis C
Brite
KEGG Orthology (KO) [BR:
pps00001
]
09120 Genetic Information Processing
09125 Information processing in viruses
03272 Virion - Hepatitis viruses
100978259 (CLDN10)
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecule (CAM) interaction
100978259 (CLDN10)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04530 Tight junction
100978259 (CLDN10)
09150 Organismal Systems
09151 Immune system
04670 Leukocyte transendothelial migration
100978259 (CLDN10)
09158 Development and regeneration
04382 Cornified envelope formation
100978259 (CLDN10)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
100978259 (CLDN10)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
pps03037
]
100978259 (CLDN10)
04147 Exosome [BR:
pps04147
]
100978259 (CLDN10)
Cilium and associated proteins [BR:
pps03037
]
Other cilia and associated proteins
Stereociliary proteins
100978259 (CLDN10)
Exosome [BR:
pps04147
]
Exosomal proteins
Exosomal proteins of ovarian cancer cells
100978259 (CLDN10)
Exosomal proteins of colorectal cancer cells
100978259 (CLDN10)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
DUF2207_C
Motif
Other DBs
NCBI-GeneID:
100978259
NCBI-ProteinID:
XP_003832075
Ensembl:
ENSPPAG00000043676
UniProt:
A0A2R9CSD6
LinkDB
All DBs
Position
14:96965336..97110530
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AA seq
228 aa
AA seq
DB search
MASTASEIIAFMVSISGWVLVSSTLPTDYWKVSTIDGTVITTATYWANLWKACVTDSTGV
SNCKDFPSMLALDGYIQACRGLMIAAVSLGFFGSIFALFGMKCTKVGGSDKAKAKIACLA
GIVFILSGLCSMTGCSLYANKITTEFFDPLFVEQKYELGAALFIGWAGASLCIIGGVIFC
FSISDNNKTPRYTYNGATSVMSSRTKYHGGEDFKTTNPSKQFDKNAYV
NT seq
687 nt
NT seq
+upstream
nt +downstream
nt
atggctagcacggcttcggagatcatcgccttcatggtctccatctcaggctgggtactg
gtgtcctccacgctgcccaccgactactggaaggtgtctaccatcgacggcacggtcatc
acaaccgccacctattgggccaacctgtggaaggcgtgcgttaccgactccacgggcgtc
tccaactgcaaggacttcccctccatgctggcgctggacggttatatccaggcatgtaga
ggacttatgatcgctgctgtcagcctgggcttctttggttccatatttgcgctctttgga
atgaagtgtaccaaagtcggaggctccgataaagccaaagctaaaattgcttgtttggct
gggattgtattcatactgtcagggctgtgctcaatgaccggctgttccctatatgcaaac
aaaatcacaacggaattctttgatcctctctttgttgagcaaaagtatgaattaggagcc
gctctgtttattggatgggcaggagcctcactgtgcataattggtggtgtcatattttgc
ttttcaatatctgacaacaacaaaacacccagatacacatacaacggggccacatctgtc
atgtcttctcggacaaagtatcatggtggagaagattttaaaacaacaaacccttcaaaa
cagtttgataaaaatgcttatgtctaa
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