Vulpes vulpes (red fox): 112907938
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Entry
112907938 CDS
T05911
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b isoform X1
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
vvp
Vulpes vulpes (red fox)
Pathway
vvp04150
mTOR signaling pathway
vvp04310
Wnt signaling pathway
vvp04390
Hippo signaling pathway
vvp04550
Signaling pathways regulating pluripotency of stem cells
vvp04916
Melanogenesis
vvp04934
Cushing syndrome
vvp05010
Alzheimer disease
vvp05022
Pathways of neurodegeneration - multiple diseases
vvp05165
Human papillomavirus infection
vvp05200
Pathways in cancer
vvp05205
Proteoglycans in cancer
vvp05217
Basal cell carcinoma
vvp05224
Breast cancer
vvp05225
Hepatocellular carcinoma
vvp05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
vvp00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
112907938 (WNT2B)
04390 Hippo signaling pathway
112907938 (WNT2B)
04150 mTOR signaling pathway
112907938 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
112907938 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
112907938 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
112907938 (WNT2B)
05205 Proteoglycans in cancer
112907938 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
112907938 (WNT2B)
05226 Gastric cancer
112907938 (WNT2B)
05217 Basal cell carcinoma
112907938 (WNT2B)
05224 Breast cancer
112907938 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
112907938 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
112907938 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
112907938 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
112907938 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
vvp00536
]
112907938 (WNT2B)
Glycosaminoglycan binding proteins [BR:
vvp00536
]
Heparan sulfate / Heparin
Morphogens
112907938 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
112907938
NCBI-ProteinID:
XP_025839071
UniProt:
A0A3Q7RAF8
LinkDB
All DBs
Position
Unknown
AA seq
393 aa
AA seq
DB search
MLEPGGAEDAAQLPPRRARAPVPTLAPGPVAPDGARASSRLGLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1182 nt
NT seq
+upstream
nt +downstream
nt
atgctggagccgggcggtgcggaggacgccgcgcagctgccccccaggcgcgcccgcgcc
cctgtgcccacgctcgcgccaggccccgtggcccccgacggcgcccgggcttcttcccgc
ctcggtcttgcctgcctgctgctgctgctgctgctgacgctgccggcccgtgtagacacg
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaacatccctggtctg
gtgagtcggcagcggcagctgtgccagcgttacccagatatcatgcgctcagtgggcgag
ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc
accacgctggaccgggaccacactgtctttggccgagtcatgctcagaagtagccgggaa
gcagcatttgtatatgccatctcatcagcaggggtggtccatgctatcacccgtgcctgt
agccagggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgac
caacgtggggattttgactggggtggctgcagtgacaacatccactatggtgttcgtttt
gccaaggcctttgtggacgccaaggaaaagaggcttaaggatgcccgggccctcatgaac
ttacataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctcgagtgtaag
tgccatggcgtaagtggctcctgtactctacgcacctgctggcgtgcgctctcagacttc
cgccgcacaggtgactacctgcggcggcgctatgatggtgctgtgcaggtgacagcaacc
caggatggtgccaacttcacagcagcccgccaaggctaccgccgtgccacccggactgac
cttgtctactttgacaactccccagattactgtgtcttggacaaggctgcaggttcccta
ggcactgcgggccgagtctgcagcaagacatctaaagggacagatggttgtgaaatcatg
tgctgtggccgaggatatgacacaactcgagtcacccgtgtcacccagtgtgaatgcaaa
ttccactggtgctgtgcagtgcggtgcaaggagtgcagaaacactgtggacgtccatact
tgcaaggcccccaagaaggcagagtggctggaccagacctga
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