Ursus maritimus (polar bear): 103658927
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Entry
103658927 CDS
T03271
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
umr
Ursus maritimus (polar bear)
Pathway
umr04150
mTOR signaling pathway
umr04310
Wnt signaling pathway
umr04390
Hippo signaling pathway
umr04550
Signaling pathways regulating pluripotency of stem cells
umr04916
Melanogenesis
umr04934
Cushing syndrome
umr05010
Alzheimer disease
umr05022
Pathways of neurodegeneration - multiple diseases
umr05165
Human papillomavirus infection
umr05200
Pathways in cancer
umr05205
Proteoglycans in cancer
umr05217
Basal cell carcinoma
umr05224
Breast cancer
umr05225
Hepatocellular carcinoma
umr05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
umr00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
103658927 (WNT8B)
04390 Hippo signaling pathway
103658927 (WNT8B)
04150 mTOR signaling pathway
103658927 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
103658927 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
103658927 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
103658927 (WNT8B)
05205 Proteoglycans in cancer
103658927 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
103658927 (WNT8B)
05226 Gastric cancer
103658927 (WNT8B)
05217 Basal cell carcinoma
103658927 (WNT8B)
05224 Breast cancer
103658927 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
103658927 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
103658927 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
103658927 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
103658927 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
umr00536
]
103658927 (WNT8B)
Glycosaminoglycan binding proteins [BR:
umr00536
]
Heparan sulfate / Heparin
Morphogens
103658927 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
103658927
NCBI-ProteinID:
XP_008684660
UniProt:
A0A384BR83
LinkDB
All DBs
Position
Unknown
AA seq
336 aa
AA seq
DB search
MGASDSRRSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAWDRWNCPERALQLSSH
GGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQLGGQGWLWGGCSDN
VGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTCKCHGVSGSCTTQTCW
LQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRSISTRELVHLEDSPDY
CLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEERRAETVSSCNCKFHW
CCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRKP
NT seq
1011 nt
NT seq
+upstream
nt +downstream
nt
atgggggcaagtgacagcagaaggtcagtgaacaatttcctgatgaccggtccaaaggct
tacctgatctattccagcagtgtggcagctggtgcccagagtggtattgaagaatgcaag
tatcagtttgcctgggaccgatggaactgccccgagagagccctccagctgtctagccat
ggtggccttcgcagtgctaatcgggagacagcgtttgtacacgccatcagttctgctggg
gtcatgtacactctgactaggaactgcagcctgggggactttgacaactgtggctgtgac
gactcccgaaatgggcagctgggcggccaaggctggctgtggggaggctgcagtgacaac
gtgggcttcggagaggcaatatccaagcagttcgtcgatgccctagagacaggacaagat
gcccgggcagccatgaacctgcacaacaacgaggccggccgcaaggcggtgaagggcacc
atgaaacgcacgtgtaagtgccacggtgtgtccggcagctgcaccacgcagacctgctgg
ctgcagctgcctgagttccgcgaggtgggcgcgcacctgaaggagaagtaccacgcggct
ctcaaggtggacctgctgcagggggctggcaacagtgccgccggccgaggcgccatcgcc
gacaccttccgctccatctccacacgggagctggtgcacttggaggactccccggactac
tgcctggagaacaaaacgctgggactgctgggtaccgagggccgagagtgcctgcggcgc
ggccgggccctgggccgctgggagcgccgcagctgccgccggctctgcggggactgcggc
ctggcggtggaggagcgccgcgccgagaccgtgtccagctgcaactgcaagttccactgg
tgctgcgcggtccgctgcgagcagtgccgccggcgcgttaccaagtacttctgcagccgc
gccgagcgaccgcgggggggcgcggcgcacaaacccgggagaaaaccctga
DBGET
integrated database retrieval system