Felis catus (domestic cat): 101096357
Help
Entry
101096357 CDS
T02385
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
fca
Felis catus (domestic cat)
Pathway
fca04150
mTOR signaling pathway
fca04310
Wnt signaling pathway
fca04390
Hippo signaling pathway
fca04550
Signaling pathways regulating pluripotency of stem cells
fca04916
Melanogenesis
fca04934
Cushing syndrome
fca05010
Alzheimer disease
fca05022
Pathways of neurodegeneration - multiple diseases
fca05165
Human papillomavirus infection
fca05200
Pathways in cancer
fca05205
Proteoglycans in cancer
fca05217
Basal cell carcinoma
fca05224
Breast cancer
fca05225
Hepatocellular carcinoma
fca05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
fca00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
101096357 (WNT8B)
04390 Hippo signaling pathway
101096357 (WNT8B)
04150 mTOR signaling pathway
101096357 (WNT8B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
101096357 (WNT8B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
101096357 (WNT8B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101096357 (WNT8B)
05205 Proteoglycans in cancer
101096357 (WNT8B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
101096357 (WNT8B)
05226 Gastric cancer
101096357 (WNT8B)
05217 Basal cell carcinoma
101096357 (WNT8B)
05224 Breast cancer
101096357 (WNT8B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
101096357 (WNT8B)
09164 Neurodegenerative disease
05010 Alzheimer disease
101096357 (WNT8B)
05022 Pathways of neurodegeneration - multiple diseases
101096357 (WNT8B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
101096357 (WNT8B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
fca00536
]
101096357 (WNT8B)
Glycosaminoglycan binding proteins [BR:
fca00536
]
Heparan sulfate / Heparin
Morphogens
101096357 (WNT8B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
101096357
NCBI-ProteinID:
XP_044895916
LinkDB
All DBs
Position
D2:59024474..59029488
Genome browser
AA seq
322 aa
AA seq
DB search
MTGPKAYLIYSSSVAAGAQSGIEECKYQFAWDRWNCPERALQLSSHSGLRSANRETAFVH
AISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQLGGQGWLWGGCSDNVGFGEAISKQFVDA
LETGQDARAAMNLHNNEAGRKAVKGTMKRTCKCHGVSGSCTTQTCWLQLPEFREVGAHLK
EKYHAALKVDLLQGAGNSAAGRGAIADTFRSISTRELVHLEDSPDYCLENKTLGLLGTEG
RECLRRGRALGRWERRSCRRLCGDCGLAVEERRAETVSSCNCKFHWCCAVRCEQCRRRVT
KYFCSRAERPRGGAAHKPGRKP
NT seq
969 nt
NT seq
+upstream
nt +downstream
nt
atgactggtccaaaggcttacctgatatattccagcagtgtggcagctggtgcccagagt
ggtattgaagaatgcaagtatcagtttgcctgggaccggtggaactgtcctgagagagcc
ctgcagctgtccagccatagtggccttcgcagtgctaatcgggagacagcgtttgtacat
gccatcagctctgctggggtcatgtacactctgactagaaactgcagcctcggggatttt
gacaactgtggctgtgatgactcccgcaatgggcagctggggggccaaggctggctgtgg
ggaggctgcagtgacaacgtgggcttcggagaggcaatatccaagcagttcgtcgatgcc
ctagagacaggacaggatgcccgggccgccatgaacctgcacaacaatgaggctggccgc
aaggcggtgaagggcaccatgaaacgcacgtgtaagtgccacggcgtgtccggcagctgc
accacgcagacctgctggctgcagctgcctgagttccgcgaggtgggcgcgcacctgaag
gagaagtaccacgcggctctcaaggtggacctgctgcagggtgccggcaacagtgcggcc
ggccgcggcgccatcgccgacaccttccgctccatctccacgcgggagctggtgcacctg
gaggactccccggactactgcctggagaacaaaacgctaggactgctgggcaccgaaggc
cgagagtgcctgcggcgggggcgggccctgggccgctgggagcgccgcagctgccgccgg
ctctgcggggactgcggactggcggtggaggagcgccgtgccgagaccgtgtccagctgc
aactgcaagttccactggtgctgcgccgtccgctgcgagcagtgccgccggcgggttacc
aagtacttctgcagccgcgccgagcggccgcgggggggcgcggcgcacaaacccgggaga
aagccctga
DBGET
integrated database retrieval system