Sus scrofa (pig): 100513655
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Entry
100513655 CDS
T01009
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b isoform X1
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
ssc
Sus scrofa (pig)
Pathway
ssc04150
mTOR signaling pathway
ssc04310
Wnt signaling pathway
ssc04390
Hippo signaling pathway
ssc04550
Signaling pathways regulating pluripotency of stem cells
ssc04916
Melanogenesis
ssc04934
Cushing syndrome
ssc05010
Alzheimer disease
ssc05022
Pathways of neurodegeneration - multiple diseases
ssc05165
Human papillomavirus infection
ssc05200
Pathways in cancer
ssc05205
Proteoglycans in cancer
ssc05217
Basal cell carcinoma
ssc05224
Breast cancer
ssc05225
Hepatocellular carcinoma
ssc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ssc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100513655 (WNT8B)
04390 Hippo signaling pathway
100513655 (WNT8B)
04150 mTOR signaling pathway
100513655 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100513655 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100513655 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100513655 (WNT8B)
05205 Proteoglycans in cancer
100513655 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100513655 (WNT8B)
05226 Gastric cancer
100513655 (WNT8B)
05217 Basal cell carcinoma
100513655 (WNT8B)
05224 Breast cancer
100513655 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100513655 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100513655 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
100513655 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100513655 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ssc00536
]
100513655 (WNT8B)
Glycosaminoglycan binding proteins [BR:
ssc00536
]
Heparan sulfate / Heparin
Morphogens
100513655 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100513655
NCBI-ProteinID:
XP_003125637
Ensembl:
ENSSSCG00000006164
UniProt:
A0A8D0SKN9
A0A4X1TZ80
LinkDB
All DBs
Position
14:111562278..111589897
Genome browser
AA seq
351 aa
AA seq
DB search
MLLMKPSVCIFLFTCVLQLSHTWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAW
DRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNG
QLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTC
KCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRS
ISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLSVEE
RRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPPGGAAHKPGRKP
NT seq
1056 nt
NT seq
+upstream
nt +downstream
nt
atgttgcttatgaagccttctgtgtgcatctttctttttacctgtgtcctccaactcagc
cacacctggtcagtgaacaatttcctgatgactggtccaaaggcttacctgatctactcc
agcagtgtagctgctggcgctcagagtggcattgaagaatgcaaataccagtttgcatgg
gatcgctggaactgccctgagagagccctgcagctgtccagccatggtggacttcgaagt
gctaatcgggaaacggcattcgtgcatgctatcagttctgctggggtcatgtacactctg
actagaaactgcagccttggggattttgacaattgtggctgtgatgattcccgcaatggg
caactggggggccaaggctggctgtggggaggctgcagcgacaacgtgggcttcggagag
gcaatatccaaacagttcgtagatgccctggagacaggacaggatgcccgggcagccatg
aatctacacaacaacgaggctggtcgcaaggcagtaaagggcaccatgaaacgcacatgt
aaatgccacggcgtttctggcagctgcaccacgcagacctgctggctgcagttgcccgag
ttccgagaggtgggcgcgcacttgaaagagaagtaccacgcagctctcaaggtggatctg
ctgcagggtgctggcaacagcgcggcgggccgcggcgccatcgccgacacctttcgctcc
atctccacgcgggagctggtgcacctggaggactccccggactactgcctggagaacaaa
actctaggactgctgggcaccgaaggcagagagtgcctgcggcgcggccgggccctgggc
cgctgggagcgtcgcagctgccgtcggctctgcggcgactgcggcctgtcggtggaggag
cgccgcgcggagacagtgtccagctgcaactgcaagttccactggtgctgcgcggtccgc
tgcgagcagtgccgccggcgggttaccaaatacttctgcagtcgcgcggagcggccgccg
gggggcgcggctcacaaacctgggagaaaaccctaa
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