Ailuropoda melanoleuca (giant panda): 100481665
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Entry
100481665 CDS
T01329
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b isoform X1
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
aml
Ailuropoda melanoleuca (giant panda)
Pathway
aml04150
mTOR signaling pathway
aml04310
Wnt signaling pathway
aml04390
Hippo signaling pathway
aml04550
Signaling pathways regulating pluripotency of stem cells
aml04916
Melanogenesis
aml04934
Cushing syndrome
aml05010
Alzheimer disease
aml05022
Pathways of neurodegeneration - multiple diseases
aml05165
Human papillomavirus infection
aml05200
Pathways in cancer
aml05205
Proteoglycans in cancer
aml05217
Basal cell carcinoma
aml05224
Breast cancer
aml05225
Hepatocellular carcinoma
aml05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
aml00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100481665 (WNT2B)
04390 Hippo signaling pathway
100481665 (WNT2B)
04150 mTOR signaling pathway
100481665 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100481665 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100481665 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100481665 (WNT2B)
05205 Proteoglycans in cancer
100481665 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100481665 (WNT2B)
05226 Gastric cancer
100481665 (WNT2B)
05217 Basal cell carcinoma
100481665 (WNT2B)
05224 Breast cancer
100481665 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100481665 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100481665 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
100481665 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100481665 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
aml00536
]
100481665 (WNT2B)
Glycosaminoglycan binding proteins [BR:
aml00536
]
Heparan sulfate / Heparin
Morphogens
100481665 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100481665
NCBI-ProteinID:
XP_002918296
Ensembl:
ENSAMEG00000003598
UniProt:
G1LA82
LinkDB
All DBs
Position
2:79130247..79148501
Genome browser
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
cccgtccccgcgctcgcgccaggacccgctgcccccgacggctctcgggcttcggcccgc
ctcggtctcgcctgcctgctgctgctgctgctgctgacgctgccggcccgcgtagacaca
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaatatccctggtctg
gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcagtgggcgag
ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc
accacgctggaccgggaccacactgtctttgggcgcgtcatgctcagaagcagccgggag
gcagcatttgtatatgccatctcgtcggcaggggtggtccatgctatcacccgtgcctgc
agccagggtgaactgagtgtgtgcagctgtgacccctacactcgtggccgacaccatgac
caacgtggggattttgactggggtggctgcagtgacaacatccactatggtgttcgcttt
gccaaggcctttgtggatgccaaggaaaagaggcttaaggatgcccgggccctcatgaat
ttacataacaaccgctgtggtcgcacggctgtgaggcggtttctgaaactcgagtgcaag
tgccacggcgtaagtggctcctgtaccctgcgcacctgctggcgtgcactctcagacttc
cgccgcacgggtgactatctgcggcggcgctatgatggcgccgtgcaggtgacagcaacc
caggatggcgccaacttcacggcagcccgccaaggctatcgccgtgccacccggactgac
cttgtctactttgacaactccccagactactgtgtcttggacaaggctgcaggttcccta
ggcactgcgggccgtgtctgcagcaagacatctaaagggacggatggttgcgaaatcatg
tgctgtggccgagggtatgacacaactcgagtcacccgcgtcacccagtgtgagtgcaaa
ttccactggtgctgtgcggtgcggtgcaaggagtgcagaaacactgtcgacgtccatact
tgcaaggcccccaagaaggcagagtggctggaccagacctga
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