Pan paniscus (bonobo): 100993261
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Entry
100993261 CDS
T02283
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b isoform X1
KO
K01064
wingless-type MMTV integration site family, member 9
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
100993261 (WNT9B)
04390 Hippo signaling pathway
100993261 (WNT9B)
04150 mTOR signaling pathway
100993261 (WNT9B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100993261 (WNT9B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100993261 (WNT9B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100993261 (WNT9B)
05205 Proteoglycans in cancer
100993261 (WNT9B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100993261 (WNT9B)
05226 Gastric cancer
100993261 (WNT9B)
05217 Basal cell carcinoma
100993261 (WNT9B)
05224 Breast cancer
100993261 (WNT9B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100993261 (WNT9B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100993261 (WNT9B)
05022 Pathways of neurodegeneration - multiple diseases
100993261 (WNT9B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100993261 (WNT9B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pps00536
]
100993261 (WNT9B)
Glycosaminoglycan binding proteins [BR:
pps00536
]
Heparan sulfate / Heparin
Morphogens
100993261 (WNT9B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
100993261
NCBI-ProteinID:
XP_057156240
Ensembl:
ENSPPAG00000033174
LinkDB
All DBs
Position
19:complement(18130185..18165182)
Genome browser
AA seq
357 aa
AA seq
DB search
MRPPPALALAGLCLLALPAAAASYFGLTGREVLTPFPGLGTAAAPAQGGAHLKQCDLLKL
SRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFLY
AVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGSK
RGNKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLKL
RYDSAVKVSSATNEALGRLELWAPARQGSLTKGLAPRSGDLVYMEDSPSFCRPSKYSPGT
AGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELVYTCKH
NT seq
1074 nt
NT seq
+upstream
nt +downstream
nt
atgcgccccccgcccgcgctggccctggccgggctctgcctgctggcgctgcccgccgcc
gccgcctcctacttcggcctgaccgggcgggaagtcctgacgcccttcccaggattgggc
actgcggcggccccggcacagggcggggcccacctgaagcagtgtgacctgctgaagctg
tcccggcggcagaagcagctctgccggagggagcccggcctggctgagaccctgagggat
gctgcgcaccttggcctgcttgagtgccagtttcagttccggcatgagcgctggaactgt
agcctggagggcaggacaggcctgctcaagagaggcttcaaagagacagctttcctgtac
gcggtgtcctctgctgccctcacccacaccctggcccgggcctgcagcgctgggcgcatg
gagcgctgcacctgtgatgactctccggggctggagagccggcaggcctggcagtggggc
gtgtgcggtgacaacctcaagtacagcaccaagtttctgagcaacttcctggggtccaag
agaggaaacaaggacctgcgggcacgggcagacgcccacaatacccacgtgggcatcaag
gctgtgaagagtggcctcaggaccacgtgtaagtgccatggcgtatcaggctcctgtgcc
gtgcgcacctgctggaagcagctctccccgttccgtgagacgggccaggtgctgaaactg
cgctatgactcggctgtcaaggtgtccagtgccaccaatgaggccttgggccgcctagag
ctgtgggcccctgccaggcagggcagcctcaccaaaggcctggccccaaggtctggggac
ctggtctacatggaggactcacccagcttctgccggcccagcaagtactcacctggcaca
gcaggtagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggctat
gacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgctac
gtggagtgccagcaatgtgtgcaggaggagcttgtgtacacctgcaagcactag
DBGET
integrated database retrieval system