Neogale vison (American mink): 122906111
Help
Entry
122906111 CDS
T08764
Symbol
WNT3
Name
(RefSeq) proto-oncogene Wnt-3
KO
K00312
wingless-type MMTV integration site family, member 3
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04150
mTOR signaling pathway
nvs04310
Wnt signaling pathway
nvs04390
Hippo signaling pathway
nvs04550
Signaling pathways regulating pluripotency of stem cells
nvs04916
Melanogenesis
nvs04934
Cushing syndrome
nvs05010
Alzheimer disease
nvs05022
Pathways of neurodegeneration - multiple diseases
nvs05165
Human papillomavirus infection
nvs05200
Pathways in cancer
nvs05205
Proteoglycans in cancer
nvs05206
MicroRNAs in cancer
nvs05217
Basal cell carcinoma
nvs05224
Breast cancer
nvs05225
Hepatocellular carcinoma
nvs05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
122906111 (WNT3)
04390 Hippo signaling pathway
122906111 (WNT3)
04150 mTOR signaling pathway
122906111 (WNT3)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
122906111 (WNT3)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
122906111 (WNT3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
122906111 (WNT3)
05206 MicroRNAs in cancer
122906111 (WNT3)
05205 Proteoglycans in cancer
122906111 (WNT3)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
122906111 (WNT3)
05226 Gastric cancer
122906111 (WNT3)
05217 Basal cell carcinoma
122906111 (WNT3)
05224 Breast cancer
122906111 (WNT3)
09172 Infectious disease: viral
05165 Human papillomavirus infection
122906111 (WNT3)
09164 Neurodegenerative disease
05010 Alzheimer disease
122906111 (WNT3)
05022 Pathways of neurodegeneration - multiple diseases
122906111 (WNT3)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
122906111 (WNT3)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
nvs00536
]
122906111 (WNT3)
Glycosaminoglycan binding proteins [BR:
nvs00536
]
Heparan sulfate / Heparin
Morphogens
122906111 (WNT3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
122906111
NCBI-ProteinID:
XP_044103650
LinkDB
All DBs
Position
5:complement(17341149..17389021)
Genome browser
AA seq
355 aa
AA seq
DB search
MEPHLLGLLLGLLLCGTRVLAGYPIWWSLALGQQYTSLGSQPLLCGSIPGLVPKQLRFCR
NYIEIMPSVAEGVKLGIQECQHQFRGRRWNCTTIDDSLAIFGPVLDKATRESAFVHAIAS
AGVAFAVTRSCAEGTSTICGCDSHHKGPPGEGWKWGGCSEDADFGVLVSREFADARENRP
DARSAMNKHNNEAGRTTILDHMHLKCKCHGLSGSCEVKTCWWAQPDFRAIGDFLKDKYDS
ASEMVVEKHRESRGWVETLRAKYALFKPPTERDLVYYENSPNFCEPNPETGSFGTRDRTC
NVTSHGIDGCDLLCCGRGHNTRTEKRKEKCHCIFHWCCYVSCQECVRIYDVHTCK
NT seq
1068 nt
NT seq
+upstream
nt +downstream
nt
atggagccccacctgctcgggctgctcctcggcctcctgctctgtggcaccagggtcctc
gccggctacccaatttggtggtccctggccctgggccagcaatacacatccctgggctca
cagcccctgctctgcggctccatcccgggcctggtccccaagcagctgcgcttctgccgg
aattacatcgagatcatgcccagtgtggccgagggcgtgaaactgggcatccaggagtgc
cagcaccagttccggggccgccgctggaactgtaccaccatagacgacagcctggccatc
ttcgggcccgtcctggacaaagccacccgtgagtcggccttcgtgcacgccattgcctct
gccggtgtggccttcgccgtcacgcgctcctgtgctgagggcacctccaccatctgcggc
tgtgactcgcaccacaaagggccgcctggcgagggctggaagtggggcggctgcagcgag
gacgccgacttcggggtgctcgtgtcccgggagttcgcagacgcgcgggagaacaggcca
gacgcgcgctcggccatgaacaagcacaacaatgaggcgggccgcacgaccatcctggac
cacatgcacctcaagtgcaagtgccacgggctgtccggcagctgcgaggtcaagacctgc
tggtgggcccaacccgacttccgcgctatcggcgacttcctcaaggacaagtacgacagt
gcctcggagatggtggtggagaagcaccgtgaatcccgcggctgggtggagaccctccgt
gccaagtatgcgctgttcaagccgcccaccgagagggacctggtctactacgagaactcc
cccaacttctgcgagcccaaccccgagacgggctcctttggcaccagggaccggacttgc
aatgtcacctcccacggcatcgacggctgcgacctactgtgctgcggccgcggccacaac
acgaggacggagaagcggaaggagaaatgccactgcatcttccactggtgctgctacgtg
agctgccaggagtgcgtccgcatctacgatgtgcacacctgcaagtag
DBGET
integrated database retrieval system