Ursus arctos (brown bear): 113244420
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Entry
113244420 CDS
T05909
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
uah
Ursus arctos (brown bear)
Pathway
uah04150
mTOR signaling pathway
uah04310
Wnt signaling pathway
uah04390
Hippo signaling pathway
uah04550
Signaling pathways regulating pluripotency of stem cells
uah04916
Melanogenesis
uah04934
Cushing syndrome
uah05010
Alzheimer disease
uah05022
Pathways of neurodegeneration - multiple diseases
uah05165
Human papillomavirus infection
uah05200
Pathways in cancer
uah05205
Proteoglycans in cancer
uah05217
Basal cell carcinoma
uah05224
Breast cancer
uah05225
Hepatocellular carcinoma
uah05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
uah00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
113244420 (WNT2B)
04390 Hippo signaling pathway
113244420 (WNT2B)
04150 mTOR signaling pathway
113244420 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
113244420 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
113244420 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
113244420 (WNT2B)
05205 Proteoglycans in cancer
113244420 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
113244420 (WNT2B)
05226 Gastric cancer
113244420 (WNT2B)
05217 Basal cell carcinoma
113244420 (WNT2B)
05224 Breast cancer
113244420 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
113244420 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
113244420 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
113244420 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
113244420 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
uah00536
]
113244420 (WNT2B)
Glycosaminoglycan binding proteins [BR:
uah00536
]
Heparan sulfate / Heparin
Morphogens
113244420 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
113244420
NCBI-ProteinID:
XP_026339536
LinkDB
All DBs
Position
Unknown
AA seq
393 aa
AA seq
DB search
MLKPGSAEDAAQLPPRRTRAPVPALAPGPAAPDGSRASARLGLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1182 nt
NT seq
+upstream
nt +downstream
nt
atgctgaagccgggtagtgcggaggacgccgcgcagctcccccctcggcgcacccgcgcc
cctgtccccgcgctcgcgccaggacccgctgcccccgacggctctcgggcttcggcccgc
ctcggtctcgcctgcctgctgctgctgctgctgctgacgctgccggcccgcgtagacaca
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaatatccctggtctg
gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcggtgggcgag
ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc
accacgctggaccgggaccacactgtctttgggcgcgtcatgctcagaagcagccgggag
gcagcatttgtatatgccatctcgtcggcgggggtggtccatgctatcacccgtgcctgt
agccagggtgaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgac
caacgtggggattttgactggggtggctgcagtgacaacatccactatggtgttcgcttt
gccaaggcctttgtggatgccaaggaaaagaggcttaaggatgcccgggccctcatgaac
ttacataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctcgagtgcaag
tgccacggcgtaagcggctcctgtaccctgcgcacctgctggcgcgcactctcagacttc
cgccgcacgggtgactatctgcggcggcgctatgatggcgctgtgcaggtgacagcaacc
caggatggtgccaacttcacggcagcccgccaaggctatcgccgtgccacccggactgac
cttgtctactttgacaactccccagactactgtgtcttggacaaggctgcaggttcccta
ggcactgcgggccgtgtctgcagcaagacatctaaagggacggatggttgcgaaatcatg
tgctgtggccgagggtatgacacaactcgagtcacccgcgtcacccagtgtgagtgcaaa
ttccactggtgctgtgcggtgcggtgcaaagagtgcagaaacactgtcgacgtccatact
tgcaaggcccccaagaaggcagagtggctggaccagacctga
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integrated database retrieval system