Homo sapiens (human): 7484
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Entry
7484 CDS
T01001
Symbol
WNT9B, WNT14B, WNT15
Name
(RefSeq) Wnt family member 9B
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
hsa
Homo sapiens (human)
Pathway
hsa04150
mTOR signaling pathway
hsa04310
Wnt signaling pathway
hsa04390
Hippo signaling pathway
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa04916
Melanogenesis
hsa04934
Cushing syndrome
hsa05010
Alzheimer disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05165
Human papillomavirus infection
hsa05200
Pathways in cancer
hsa05205
Proteoglycans in cancer
hsa05217
Basal cell carcinoma
hsa05224
Breast cancer
hsa05225
Hepatocellular carcinoma
hsa05226
Gastric cancer
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06181
Salmonella
nt06215
WNT signaling (cancer)
nt06217
HH signaling (cancer)
nt06260
Colorectal cancer
nt06261
Gastric cancer
nt06263
Hepatocellular carcinoma
nt06269
Basal cell carcinoma
nt06270
Breast cancer
nt06271
Endometrial cancer
nt06274
Thyroid cancer
nt06505
WNT signaling
Element
N00010
Mutation-inactivated PTCH1 to Hedgehog signaling pathway
N00017
Mutation-activated SMO to Hedgehog signaling pathway
N00056
Wnt signaling pathway
N00059
FZD7-overexpression to Wnt signaling pathway
N00060
LRP6-overexpression to Wnt signaling pathway
N01442
Wnt signaling modulation, Wnt inhibitor
N01443
Wnt signaling modulation, Wnt acylation
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
7484 (WNT9B)
04390 Hippo signaling pathway
7484 (WNT9B)
04150 mTOR signaling pathway
7484 (WNT9B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
7484 (WNT9B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
7484 (WNT9B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
7484 (WNT9B)
05205 Proteoglycans in cancer
7484 (WNT9B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
7484 (WNT9B)
05226 Gastric cancer
7484 (WNT9B)
05217 Basal cell carcinoma
7484 (WNT9B)
05224 Breast cancer
7484 (WNT9B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
7484 (WNT9B)
09164 Neurodegenerative disease
05010 Alzheimer disease
7484 (WNT9B)
05022 Pathways of neurodegeneration - multiple diseases
7484 (WNT9B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
7484 (WNT9B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
hsa00536
]
7484 (WNT9B)
Glycosaminoglycan binding proteins [BR:
hsa00536
]
Heparan sulfate / Heparin
Morphogens
7484 (WNT9B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
7484
NCBI-ProteinID:
NP_003387
OMIM:
602864
HGNC:
12779
Ensembl:
ENSG00000158955
UniProt:
O14905
LinkDB
All DBs
Position
17:46833189..46886738
Genome browser
AA seq
357 aa
AA seq
DB search
MRPPPALALAGLCLLALPAAAASYFGLTGREVLTPFPGLGTAAAPAQGGAHLKQCDLLKL
SRRQKQLCRREPGLAETLRDAAHLGLLECQFQFRHERWNCSLEGRMGLLKRGFKETAFLY
AVSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGSK
RGNKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLSPFRETGQVLKL
RYDSAVKVSSATNEALGRLELWAPARQGSLTKGLAPRSGDLVYMEDSPSFCRPSKYSPGT
AGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELVYTCKH
NT seq
1074 nt
NT seq
+upstream
nt +downstream
nt
atgcgccccccgcccgcgctggccctggccgggctctgcctgctggcgctgcccgccgcc
gccgcctcctacttcggcctgaccgggcgggaagtcctgacgcccttcccaggattgggc
actgcggcagccccggcacagggcggggcccacctgaagcagtgtgacctgctgaagctg
tcccggcggcagaagcagctctgccggagggagcccggcctggctgagaccctgagggat
gctgcgcacctcggcctgcttgagtgccagtttcagttccggcatgagcgctggaactgt
agcctggagggcaggatgggcctgctcaagagaggcttcaaagagacagctttcctgtac
gcggtgtcctctgccgccctcacccacaccctggcccgggcctgcagcgctgggcgcatg
gagcgctgcacctgtgatgactctccggggctggagagccggcaggcctggcagtggggc
gtgtgcggtgacaacctcaagtacagcaccaagtttctgagcaacttcctggggtccaag
agaggaaacaaggacctgcgggcacgggcagacgcccacaatacccacgtgggcatcaag
gctgtgaagagtggcctcaggaccacgtgtaagtgccatggcgtatcaggctcctgtgcc
gtgcgcacctgctggaagcagctctccccgttccgtgagacgggccaggtgctgaaactg
cgctatgactcggctgtcaaggtgtccagtgccaccaatgaggccttgggccgcctagag
ctgtgggcccctgccaggcagggcagcctcaccaaaggcctggccccaaggtctggggac
ctggtgtacatggaggactcacccagcttctgccggcccagcaagtactcacctggcaca
gcaggtagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggctat
gacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgctac
gtggagtgccagcaatgtgtgcaggaggagcttgtgtacacctgcaagcactag
DBGET
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