Panthera pardus (leopard): 109272063
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Entry
109272063 CDS
T06062
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
ppad
Panthera pardus (leopard)
Pathway
ppad04150
mTOR signaling pathway
ppad04310
Wnt signaling pathway
ppad04390
Hippo signaling pathway
ppad04550
Signaling pathways regulating pluripotency of stem cells
ppad04916
Melanogenesis
ppad04934
Cushing syndrome
ppad05010
Alzheimer disease
ppad05022
Pathways of neurodegeneration - multiple diseases
ppad05165
Human papillomavirus infection
ppad05200
Pathways in cancer
ppad05205
Proteoglycans in cancer
ppad05217
Basal cell carcinoma
ppad05224
Breast cancer
ppad05225
Hepatocellular carcinoma
ppad05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ppad00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
109272063 (WNT2B)
04390 Hippo signaling pathway
109272063 (WNT2B)
04150 mTOR signaling pathway
109272063 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
109272063 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
109272063 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
109272063 (WNT2B)
05205 Proteoglycans in cancer
109272063 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
109272063 (WNT2B)
05226 Gastric cancer
109272063 (WNT2B)
05217 Basal cell carcinoma
109272063 (WNT2B)
05224 Breast cancer
109272063 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
109272063 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
109272063 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
109272063 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
109272063 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ppad00536
]
109272063 (WNT2B)
Glycosaminoglycan binding proteins [BR:
ppad00536
]
Heparan sulfate / Heparin
Morphogens
109272063 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
109272063
NCBI-ProteinID:
XP_019313411
Ensembl:
ENSPPRG00000016238
UniProt:
A0A9V1G1L3
LinkDB
All DBs
Position
Unknown
AA seq
393 aa
AA seq
DB search
MLKPGGAEEAAQLPPRRARAPVPVLPPGPAAPDGSRASARLGLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1182 nt
NT seq
+upstream
nt +downstream
nt
atgctgaagccgggtggtgcggaggaagccgcacagctcccccctcggcgcgcccgcgcc
cctgtccccgtgctcccgccaggacccgcggcccccgacggctctcgggcttcggcccgc
ctcggtcttgcctgcctgctgctgctgctgctgctgacgctgccggcccgcgtagacacg
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaatatccctggtctg
gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcggtgggcgag
ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc
accacgctggaccgggaccacactgtctttggccgtgtcatgctcagaagtagccgggag
gcagcatttgtatatgccatctcgtctgcaggggtggtccatgctatcactcgtgcctgc
agccagggagaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgac
caacgtggggattttgactggggtggctgcagtgacaacatccattatggtgttcgcttt
gccaaggcctttgtggatgccaaggaaaagaggcttaaggatgcccgggccctcatgaac
ttacataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctcgagtgtaag
tgccatggcgttagtggctcctgtactctgcgcacctgctggcgtgcactctcagacttc
cgccgcacaggtgattacctgcggcggcgctatgatggggctgtgcaggtgacagcaacc
caggatggcgccaacttcacagcagcccgccaaggttatcgccgtgccacccggactgac
cttgtctactttgacaactccccagactactgtgtcttagacaaggctgcaggttcccta
ggcactgcgggccgtgtctgtagcaagacatccaaagggacggatggttgcgaaatcatg
tgctgtggccgagggtacgacacaactcgagtcacccgtgtcacccagtgtgagtgcaaa
ttccactggtgctgtgcagtgcggtgcaaggagtgcagaaacactgtggacgtccacact
tgcaaggcccccaagaaggcagagtggctggaccagacctga
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