Puma yagouaroundi (jaguarundi): 121037468
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Entry
121037468 CDS
T07555
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
pyu
Puma yagouaroundi (jaguarundi)
Pathway
pyu04150
mTOR signaling pathway
pyu04310
Wnt signaling pathway
pyu04390
Hippo signaling pathway
pyu04550
Signaling pathways regulating pluripotency of stem cells
pyu04916
Melanogenesis
pyu04934
Cushing syndrome
pyu05010
Alzheimer disease
pyu05022
Pathways of neurodegeneration - multiple diseases
pyu05165
Human papillomavirus infection
pyu05200
Pathways in cancer
pyu05205
Proteoglycans in cancer
pyu05217
Basal cell carcinoma
pyu05224
Breast cancer
pyu05225
Hepatocellular carcinoma
pyu05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pyu00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
121037468 (WNT8B)
04390 Hippo signaling pathway
121037468 (WNT8B)
04150 mTOR signaling pathway
121037468 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
121037468 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
121037468 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
121037468 (WNT8B)
05205 Proteoglycans in cancer
121037468 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
121037468 (WNT8B)
05226 Gastric cancer
121037468 (WNT8B)
05217 Basal cell carcinoma
121037468 (WNT8B)
05224 Breast cancer
121037468 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
121037468 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
121037468 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
121037468 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
121037468 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pyu00536
]
121037468 (WNT8B)
Glycosaminoglycan binding proteins [BR:
pyu00536
]
Heparan sulfate / Heparin
Morphogens
121037468 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
121037468
NCBI-ProteinID:
XP_040342851
LinkDB
All DBs
Position
Unknown
AA seq
353 aa
AA seq
DB search
MAQRLASAWCVGATTKTSVWLEQSKSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQF
AWDRWNCPERALQLSSHSGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSR
NGQLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKR
TCKCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTF
RSISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAV
EERRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRKP
NT seq
1062 nt
NT seq
+upstream
nt +downstream
nt
atggcccagaggctggcgagtgcttggtgtgttggagcaacaacaaagacatcagtgtgg
ctagagcagagcaagtcagtgaacaatttcctgatgactggtccaaaggcttacctgata
tattccagcagtgtggcagctggtgcccagagtggtattgaagaatgcaagtatcagttt
gcctgggaccggtggaactgtcctgagagagccctgcagctgtccagccatagtggcctt
cgcagtgctaatcgggagacagcgtttgtacatgccatcagctctgctggggtcatgtac
actctgactagaaactgcagcctcggggattttgacaactgtggctgtgatgactcccgc
aatgggcagctggggggccaaggctggctgtggggaggctgcagtgacaacgtgggcttc
ggagaggcaatatccaagcagttcgtcgatgccctagagacaggacaggatgcccgggcc
gccatgaacctgcacaacaatgaggccggccgcaaggcggtgaagggcaccatgaaacgc
acgtgtaagtgccacggcgtgtccggcagctgcaccacacagacctgctggctgcagctg
cctgagttccgcgaggtgggcgcgcacctgaaggagaagtaccacgcggctctcaaggtg
gacctgctgcagggtgccggcaacagtgcggccggccgcggcgccatcgccgacaccttc
cgctccatctccacgcgggagctggtgcacctggaggactccccggactactgcctggag
aacaaaacgctaggactgctgggcaccgaaggccgagagtgcctgcggcgggggcgggcc
ctgggccgctgggagcgccgcagctgccgccggctctgcggggactgcggactggcggtg
gaggagcgccgtgccgagaccgtgtccagctgcaactgcaagttccactggtgctgcgcc
gtccgctgtgagcagtgccgccggcgggttaccaagtacttctgcagccgcgccgagcgg
ccgcgggggggcgcggcgcacaaacccgggagaaagccctga
DBGET
integrated database retrieval system