Pan paniscus (bonobo): 100987794
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Entry
100987794 CDS
T02283
Symbol
WNT6
Name
(RefSeq) protein Wnt-6
KO
K00445
wingless-type MMTV integration site family, member 6
Organism
pps
Pan paniscus (bonobo)
Pathway
pps04150
mTOR signaling pathway
pps04310
Wnt signaling pathway
pps04390
Hippo signaling pathway
pps04550
Signaling pathways regulating pluripotency of stem cells
pps04916
Melanogenesis
pps04934
Cushing syndrome
pps05010
Alzheimer disease
pps05022
Pathways of neurodegeneration - multiple diseases
pps05165
Human papillomavirus infection
pps05200
Pathways in cancer
pps05205
Proteoglycans in cancer
pps05217
Basal cell carcinoma
pps05224
Breast cancer
pps05225
Hepatocellular carcinoma
pps05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pps00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100987794 (WNT6)
04390 Hippo signaling pathway
100987794 (WNT6)
04150 mTOR signaling pathway
100987794 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100987794 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100987794 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100987794 (WNT6)
05205 Proteoglycans in cancer
100987794 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100987794 (WNT6)
05226 Gastric cancer
100987794 (WNT6)
05217 Basal cell carcinoma
100987794 (WNT6)
05224 Breast cancer
100987794 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100987794 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
100987794 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
100987794 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100987794 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pps00536
]
100987794 (WNT6)
Glycosaminoglycan binding proteins [BR:
pps00536
]
Heparan sulfate / Heparin
Morphogens
100987794 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
100987794
NCBI-ProteinID:
XP_034811066
Ensembl:
ENSPPAG00000010119
LinkDB
All DBs
Position
13:121492605..121507593
Genome browser
AA seq
365 aa
AA seq
DB search
MLPPAPSRLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPSGLPGTPGPPGPAGSPEGSAAWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctgccgcccgcaccctcccgcctcgggctgctgctgctgctgctcctgtgcccggcg
cacgtcggcggactgtggtgggctgtgggcagccccttggttatggaccctaccagcatc
tgcaggaaggcacggcggctggccgggcggcaggctgagttgtgccaggctgagccggaa
gtggtggcagagctagcccggggcgcccggctcggggtgcgagagtgccagttccagttc
cgcttccgccgctggaattgctccagccacagcaaggcctttggacgcatcctgcaacag
gatattcgggagacggccttcgtgttcgccatcactgctgccggcgccagccacgccgtc
acgcaggcctgttctatgggcgagctgctgcagtgcggctgccaggcgccccgcgggcgg
gcccctccccggccctccggcctgcccggcacccccggaccccctggccccgcgggctcc
ccggaaggcagcgccgcctgggagtggggaggctgcggcgacgacgtggacttcggggac
gagaagtcgaggctctttatggacgcgcggcacaagcggggacgcggagacatccgcgcg
ttggtgcaactgcacaacaacgaggcgggccggctggccgtgcggagccacacgcgcacc
gagtgcaaatgccacgggctgtcgggatcatgcgcgctgcgcacctgctggcagaagctg
cctccgtttcgcgaggtgggcgcgcggctgctggagcgcttccacggcgcctcacgcgtc
atgggcaccaacgacggcaaggccctgctgcccgccgtccgcacgctcaagccgccgggc
cgagcggacctcctctacgccgccgattcgcccgacttctgcgcccccaaccgacgcacc
ggctcccccggcacgcgcggtcgcgcctgcaatagcagcgccccggacctcagcggctgc
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcagctcgaagagaactgc
ctgtgccgcttccactggtgctgcgtagtacagtgccaccgctgccgtgtgcgcaaggag
ctcagcctctgcctctga
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integrated database retrieval system