Phascolarctos cinereus (koala): 110213976
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Entry
110213976 CDS
T05867
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
pcw
Phascolarctos cinereus (koala)
Pathway
pcw04150
mTOR signaling pathway
pcw04310
Wnt signaling pathway
pcw04390
Hippo signaling pathway
pcw04550
Signaling pathways regulating pluripotency of stem cells
pcw04916
Melanogenesis
pcw04934
Cushing syndrome
pcw05010
Alzheimer disease
pcw05022
Pathways of neurodegeneration - multiple diseases
pcw05165
Human papillomavirus infection
pcw05200
Pathways in cancer
pcw05205
Proteoglycans in cancer
pcw05217
Basal cell carcinoma
pcw05224
Breast cancer
pcw05225
Hepatocellular carcinoma
pcw05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pcw00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
110213976 (WNT8B)
04390 Hippo signaling pathway
110213976 (WNT8B)
04150 mTOR signaling pathway
110213976 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
110213976 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
110213976 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
110213976 (WNT8B)
05205 Proteoglycans in cancer
110213976 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
110213976 (WNT8B)
05226 Gastric cancer
110213976 (WNT8B)
05217 Basal cell carcinoma
110213976 (WNT8B)
05224 Breast cancer
110213976 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
110213976 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
110213976 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
110213976 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
110213976 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pcw00536
]
110213976 (WNT8B)
Glycosaminoglycan binding proteins [BR:
pcw00536
]
Heparan sulfate / Heparin
Morphogens
110213976 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
110213976
NCBI-ProteinID:
XP_020850217
UniProt:
A0A6P5KXX5
LinkDB
All DBs
Position
Unknown
AA seq
385 aa
AA seq
DB search
MTCEQRWHSQKVGVGGNSIPFSLRSSSLLPGSQVSILGLFLMEPPAYIFLFTCVLQLSHT
WSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAWDRWNCPERALQLSSHGGLRSAN
RETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQLGGQGWLWGGCSDNVGFGEAI
SKQFVDALETGQDARAAMNLHNNEAGRKAVKATMKRTCKCHGVSGSCTTQTCWLQLPEFR
EVGAHLKEKYHAALKVELLQGAGNSAAGRGAIADTFRAISTRELVHLEDSPDYCLENKTL
GLPGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEQRRAETVTSCNCKFHWCCAVRCE
QCRRRVTKYFCSRSAGERLRPRRRP
NT seq
1158 nt
NT seq
+upstream
nt +downstream
nt
atgacctgtgaacagaggtggcattctcagaaagttggggttggaggaaattccatcccc
ttctcgctgaggagctcatctctgctccctggatcgcaagtctccatcctgggactgttt
ctcatggagcccccagcctatatcttccttttcacttgtgtcctccagctcagccatacc
tggtcagtcaataatttcctgatgactggtccaaaggcctatctgatctactccagcagt
gtggctgctggcgctcagagtggcattgaagaatgtaaataccagtttgcctgggaccga
tggaactgcccggagagagcgctccagctgtccagtcatggcgggctacgcagtgccaat
cgagagacagcctttgtacatgctatcagctctgctggggtcatgtacacgttgacccga
aactgcagccttggggattttgacaactgtggatgtgacgattcccgaaatgggcagctg
gggggccagggctggctatggggtggctgcagtgacaacgtgggctttggagaggccatc
tccaaacaatttgtggatgcactggagactgggcaggatgcccgggctgccatgaactta
cacaacaatgaagctggccgcaaggcggtgaaggccaccatgaagcgcacgtgcaaatgt
cacggcgtgtcaggcagctgcaccactcagacgtgctggctgcagctgcccgagtttcgc
gaggtgggcgcgcacctcaaggagaagtatcacgcggcgctcaaggtggagctgctgcag
ggcgcaggcaacagcgcggcgggacgcggagccatcgccgacaccttccgcgctatctcc
acgcgcgagctcgtgcacctggaagactcgcccgactactgcctggagaacaagacgctc
ggcctgccaggcactgaaggccgcgagtgcctgcggcgcggtcgcgccctgggccgctgg
gagcgccgcagctgccgccgcctgtgcggagactgcgggctggcggtggagcagcggcgc
gccgagaccgtgaccagctgcaactgcaagtttcactggtgctgcgccgtgcgctgcgag
cagtgtcgccgccgcgtcaccaagtacttctgcagccgctcggctggagagcggctgcgt
cccaggaggcggccctag
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