Rattus norvegicus (rat): 116466
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Entry
116466 CDS
T01003
Symbol
Wnt2b
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
rno
Rattus norvegicus (rat)
Pathway
rno04150
mTOR signaling pathway
rno04310
Wnt signaling pathway
rno04390
Hippo signaling pathway
rno04550
Signaling pathways regulating pluripotency of stem cells
rno04916
Melanogenesis
rno04934
Cushing syndrome
rno05010
Alzheimer disease
rno05022
Pathways of neurodegeneration - multiple diseases
rno05165
Human papillomavirus infection
rno05200
Pathways in cancer
rno05205
Proteoglycans in cancer
rno05217
Basal cell carcinoma
rno05224
Breast cancer
rno05225
Hepatocellular carcinoma
rno05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
rno00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
116466 (Wnt2b)
04390 Hippo signaling pathway
116466 (Wnt2b)
04150 mTOR signaling pathway
116466 (Wnt2b)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
116466 (Wnt2b)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
116466 (Wnt2b)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
116466 (Wnt2b)
05205 Proteoglycans in cancer
116466 (Wnt2b)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
116466 (Wnt2b)
05226 Gastric cancer
116466 (Wnt2b)
05217 Basal cell carcinoma
116466 (Wnt2b)
05224 Breast cancer
116466 (Wnt2b)
09172 Infectious disease: viral
05165 Human papillomavirus infection
116466 (Wnt2b)
09164 Neurodegenerative disease
05010 Alzheimer disease
116466 (Wnt2b)
05022 Pathways of neurodegeneration - multiple diseases
116466 (Wnt2b)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
116466 (Wnt2b)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
rno00536
]
116466 (Wnt2b)
Glycosaminoglycan binding proteins [BR:
rno00536
]
Heparan sulfate / Heparin
Morphogens
116466 (Wnt2b)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
116466
NCBI-ProteinID:
NP_001178777
RGD:
69346
Ensembl:
ENSRNOG00000014385
UniProt:
A6K3Q3
G3V7U3
LinkDB
All DBs
Position
2:complement(195142573..195156945)
Genome browser
AA seq
391 aa
AA seq
DB search
MLKPRGEDEAAQLAPRRARVPVAALRPAPPDVSPASARLGLACLLLLLLLTLPARVDTSW
WYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNCTT
LDRDHTVFGRAMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHDQR
GDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECKCH
GVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRHATRTDLV
YFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECKFH
WCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1176 nt
NT seq
+upstream
nt +downstream
nt
atgctgaagccgcggggtgaggacgaagccgcgcagctcgcccctcggcgtgcccgcgtc
ccggtcgccgcgttaagacccgcgccccccgacgtgtccccagcttctgcccgtctgggt
cttgcctgtctgctgctgctgctgcttctgactctgccggcccgtgtagacacgtcctgg
tggtacataggggcactgggagcccgagtgatctgtgacaacatcccgggtctggtgagc
cggcagcggcagctgtgtcagcgctacccagacatcatgcgctcagtaggagaaggtgcc
cgggaatggatccgagagtgtcaacaccagttccgtcatcaccgctggaattgcaccaca
ctggaccgggaccacactgtctttggccgtgctatgctcagaagcagtcgggaggcagcg
tttgtctatgctatctcatcagcaggagtggtccatgctatcactcgggcctgcagccag
ggtgagctgagtgtgtgcagctgtgacccatatacccgtggtcggcaccatgatcaacga
ggggactttgactggggtggctgtagtgacaacatccactatggtgtccgctttgccaag
gcttttgtggatgccaaagagaagaggcttaaggatgcccgggccctcatgaacttacat
aacaaccgctgcggtcgcacggctgtacggcgatttctgaagctggagtgcaagtgtcat
ggtgtgagtggctcctgtaccctgcgcacctgctggagggcactctcagacttccgccgt
accggtgactacctgaggaggcgatatgatggggctgtgcaggtgacagccacacaggat
ggggccaacttcacagcagcccgccaaggctatcgccatgccacccggactgatcttgtc
tactttgacaactcccctgactactgtgtcttggacaaggctgcaggttccctaggtacc
gcaggccgcgtctgcagcaagacttctaaaggaacagatgggtgtgaaatcatgtgttgc
ggccgaggatatgacacaactcgggtcacccgggtcacccagtgtgagtgcaaattccac
tggtgctgtgctgtgcggtgcaaggagtgcagaaacactgtggatgtccacacgtgcaag
gcccctaagaaggcagagtggctggaccagacctga
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