Equus caballus (horse): 100070360
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Entry
100070360 CDS
T01058
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
ecb
Equus caballus (horse)
Pathway
ecb04150
mTOR signaling pathway
ecb04310
Wnt signaling pathway
ecb04390
Hippo signaling pathway
ecb04550
Signaling pathways regulating pluripotency of stem cells
ecb04916
Melanogenesis
ecb04934
Cushing syndrome
ecb05010
Alzheimer disease
ecb05022
Pathways of neurodegeneration - multiple diseases
ecb05165
Human papillomavirus infection
ecb05200
Pathways in cancer
ecb05205
Proteoglycans in cancer
ecb05217
Basal cell carcinoma
ecb05224
Breast cancer
ecb05225
Hepatocellular carcinoma
ecb05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ecb00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100070360 (WNT8B)
04390 Hippo signaling pathway
100070360 (WNT8B)
04150 mTOR signaling pathway
100070360 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100070360 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100070360 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100070360 (WNT8B)
05205 Proteoglycans in cancer
100070360 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100070360 (WNT8B)
05226 Gastric cancer
100070360 (WNT8B)
05217 Basal cell carcinoma
100070360 (WNT8B)
05224 Breast cancer
100070360 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100070360 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100070360 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
100070360 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100070360 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100070360 (WNT8B)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100070360 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100070360
NCBI-ProteinID:
XP_005602618
Ensembl:
ENSECAG00000009521
VGNC:
25051
UniProt:
A0A9L0RAJ6
LinkDB
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Position
1:complement(29517072..29544163)
Genome browser
AA seq
351 aa
AA seq
DB search
MFLMKPSVCIFLFTCVLQLSHTWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAW
DRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNG
QLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTC
KCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRS
ISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEE
RRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRTP
NT seq
1056 nt
NT seq
+upstream
nt +downstream
nt
atgtttcttatgaagccttctgtgtgcatctttcttttcacctgtgtcctccaactcagc
cacacctggtcagtgaacaatttcctgatgactggtccaaaggcttacctgatctactcc
agcagtgtggcagctggtgcccagagtggtattgaagaatgcaagtaccagttcgcctgg
gaccgctggaactgccctgagagagccctgcagctatccagccatggcggccttcgcagt
gctaatcgggagacagcatttgtacatgccatcagttctgctggtgtcatgtacactctg
accagaaactgcagccttggggattttgacaactgtggctgtgatgactcccgcaacgga
caactagggggccaaggctggctgtgggggggctgcagtgacaacgtgggcttcggagag
gcaatatccaagcagttcgtggatgccctggagacaggacaggatgcccgggcagccatg
aacctgcacaacaacgaggctggccgcaaggctgtgaagggcaccatgaaacgcacgtgt
aagtgccacggcgtgtctggcagctgcaccacacagacctgctggctgcagctgcccgag
ttccgcgaggtgggcgcgcacctgaaggagaagtaccatgcagctctcaaggtggacctg
ctgcagggcgctggcaacagcgcggccggccgcggcgctatagccgacaccttccgctcc
atctccacgcgggagctggtgcacttggaggactccccggactactgcctggagaacaaa
acgctaggactgctgggcaccgaaggccgagagtgcctgcggcgcgggcgggccctgggc
cgctgggagcgccgcagctgccgccggctgtgcggggactgcgggctggcggtggaggaa
cgtcgcgccgagaccgtgtccagctgcaactgcaagttccactggtgctgcgctgtccgc
tgcgagcagtgccgccggcgggtcaccaagtacttctgtagccgcgcggagcggccgcgg
gggggcgcggcgcacaaacccgggagaacaccctaa
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integrated database retrieval system