Capra hircus (goat): 102176193
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Entry
102176193 CDS
T02910
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
chx
Capra hircus (goat)
Pathway
chx04150
mTOR signaling pathway
chx04310
Wnt signaling pathway
chx04390
Hippo signaling pathway
chx04550
Signaling pathways regulating pluripotency of stem cells
chx04916
Melanogenesis
chx04934
Cushing syndrome
chx05010
Alzheimer disease
chx05022
Pathways of neurodegeneration - multiple diseases
chx05165
Human papillomavirus infection
chx05200
Pathways in cancer
chx05205
Proteoglycans in cancer
chx05217
Basal cell carcinoma
chx05224
Breast cancer
chx05225
Hepatocellular carcinoma
chx05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
chx00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102176193 (WNT8B)
04390 Hippo signaling pathway
102176193 (WNT8B)
04150 mTOR signaling pathway
102176193 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102176193 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102176193 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102176193 (WNT8B)
05205 Proteoglycans in cancer
102176193 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102176193 (WNT8B)
05226 Gastric cancer
102176193 (WNT8B)
05217 Basal cell carcinoma
102176193 (WNT8B)
05224 Breast cancer
102176193 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102176193 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
102176193 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
102176193 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102176193 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
chx00536
]
102176193 (WNT8B)
Glycosaminoglycan binding proteins [BR:
chx00536
]
Heparan sulfate / Heparin
Morphogens
102176193 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
102176193
NCBI-ProteinID:
XP_017897005
UniProt:
A0A8C2RUY4
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All DBs
Position
26:complement(30304225..30335373)
Genome browser
AA seq
350 aa
AA seq
DB search
MLVKPSACIFLFTCVFQLSHTWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAWD
RWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQ
LGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTCK
CHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRSI
STWELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEER
RAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRADRPRGGAAHEPGRKP
NT seq
1053 nt
NT seq
+upstream
nt +downstream
nt
atgcttgtgaagccttctgcgtgcatctttcttttcacctgtgtcttccaactcagccat
acctggtcagtgaacaatttcctgatgactggtccaaaggcttacctgatctactccagc
agcgtggcagctggtgcccagagtggaattgaagaatgcaaataccagtttgcttgggac
cgctggaactgccctgagagagccctgcagctgtccagccatggtggccttcgcagtgct
aatcgggagacagcgtttgtgcacgccatcagttctgccggggtcatgtacactctgact
agaaactgcagccttggggattttgacaactgtggctgtgatgactcccgcaatgggcaa
ctggggggccaaggctggctgtggggaggctgcagcgacaacgtgggcttcggagaggca
atatccaagcagttcgtcgatgccctggagacaggacaggatgctcgggcagctatgaac
ctgcacaacaacgaggccggccgcaaggcggtgaagggcaccatgaaacgcacgtgcaag
tgccacggggtgtctggcagctgcaccacgcagacctgctggctgcagctgccggagttc
cgagaggtgggcgcgcacctgaaagagaagtaccacgcagctctcaaggtggacctgctg
cagggtgcaggcaacagcgcggcgggccgcggcgccatcgctgacacctttcgctccatc
tccacgtgggagctggtgcacctggaggactccccggactactgcctggagaacaagacg
ctagggctgctgggcaccgaaggcagagagtgcctgcggcgcggccgggccctgggccgc
tgggagcgccgcagctgccgccgactctgcggggactgcgggctggcggtagaggagcgc
cgcgccgagaccgtgtccagctgcaactgcaagtttcactggtgctgcgcggtgcgctgc
gagcagtgccgccggcgagtcaccaagtacttctgcagccgcgcggaccggccacggggg
ggcgcggcgcacgaacccgggagaaaaccctaa
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