Camelus dromedarius (Arabian camel): 105084321
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Entry
105084321 CDS
T04642
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
cdk
Camelus dromedarius (Arabian camel)
Pathway
cdk04150
mTOR signaling pathway
cdk04310
Wnt signaling pathway
cdk04390
Hippo signaling pathway
cdk04550
Signaling pathways regulating pluripotency of stem cells
cdk04916
Melanogenesis
cdk04934
Cushing syndrome
cdk05010
Alzheimer disease
cdk05022
Pathways of neurodegeneration - multiple diseases
cdk05165
Human papillomavirus infection
cdk05200
Pathways in cancer
cdk05205
Proteoglycans in cancer
cdk05217
Basal cell carcinoma
cdk05224
Breast cancer
cdk05225
Hepatocellular carcinoma
cdk05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
cdk00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
105084321 (WNT8B)
04390 Hippo signaling pathway
105084321 (WNT8B)
04150 mTOR signaling pathway
105084321 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
105084321 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
105084321 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
105084321 (WNT8B)
05205 Proteoglycans in cancer
105084321 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
105084321 (WNT8B)
05226 Gastric cancer
105084321 (WNT8B)
05217 Basal cell carcinoma
105084321 (WNT8B)
05224 Breast cancer
105084321 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
105084321 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
105084321 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
105084321 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
105084321 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
cdk00536
]
105084321 (WNT8B)
Glycosaminoglycan binding proteins [BR:
cdk00536
]
Heparan sulfate / Heparin
Morphogens
105084321 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
105084321
NCBI-ProteinID:
XP_031316607
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All DBs
Position
11:59023766..59028934
Genome browser
AA seq
335 aa
AA seq
DB search
MPAFSNHHPDQSAVISIEAYLIYSSSVAAGAQSGIEECKYQFAWDRWNCPERALQLSSHG
GLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQLGGQGWLWGGCSDNV
GFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTCKCHGVSGSCTTQTCWL
QLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRSISTRELVHLEDSPDYC
LENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEERRAETVSSCNCKFHWC
CAVRCEQCRRRVTKYFCSRAERPRGGAVHTPGRKP
NT seq
1008 nt
NT seq
+upstream
nt +downstream
nt
atgccagccttcagcaaccaccaccctgatcagtcagcagtcatcagcatcgaggcttac
ctgatctactccagcagcgtggcagcaggtgctcagagtggtattgaagaatgcaaatac
cagtttgcctgggaccgctggaactgccctgagagagccctgcagctgtccagccatggc
ggccttcgcagtgctaatcgggagacagcatttgtacatgccatcagttctgctggggtc
atgtacactctgactagaaactgcagccttggggattttgacaactgtggctgtgatgac
tcccgcaatgggcaactggggggccaaggctggctgtggggaggctgcagcgacaacgtg
ggctttggagaggcaatatccaagcagttcgtcgatgccctggagacaggacaggatgcc
cgggcagccatgaacctacacaacaacgaggctggccgcaaggcggtgaagggcaccatg
aaacgcacgtgtaagtgtcatggcgtgtcaggtagctgcaccacgcagacctgctggctg
cagctgcccgagttccgcgaggtgggcgcacacctgaaagagaagtaccacgcagctctc
aaggtggacctgttgcagggtgctggtaatagcgcggccggccgcggcgccatcgccgac
acctttcgctccatctccacgcgggaactggtgcacctggaggactccccagactactgc
ctggagaacaaaacgcttggactgctgggcaccgaaggcagagagtgcttgcggcgcggc
cgggccctcggacgctgggaacgccgcagttgccgtcggctgtgcggggactgcgggctg
gcggtggaggagcgccgcgccgagacggtgtccagttgcaactgcaagttccactggtgc
tgcgcggtccgctgcgagcagtgccgtcggcgggtcaccaagtatttctgcagccgcgcg
gagcggccgcgggggggcgcggtgcacacacccgggagaaaaccctaa
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integrated database retrieval system