Phascolarctos cinereus (koala): 110218849
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Entry
110218849 CDS
T05867
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
pcw
Phascolarctos cinereus (koala)
Pathway
pcw04150
mTOR signaling pathway
pcw04310
Wnt signaling pathway
pcw04390
Hippo signaling pathway
pcw04550
Signaling pathways regulating pluripotency of stem cells
pcw04916
Melanogenesis
pcw04934
Cushing syndrome
pcw05010
Alzheimer disease
pcw05022
Pathways of neurodegeneration - multiple diseases
pcw05165
Human papillomavirus infection
pcw05200
Pathways in cancer
pcw05205
Proteoglycans in cancer
pcw05217
Basal cell carcinoma
pcw05224
Breast cancer
pcw05225
Hepatocellular carcinoma
pcw05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pcw00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
110218849 (WNT2B)
04390 Hippo signaling pathway
110218849 (WNT2B)
04150 mTOR signaling pathway
110218849 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
110218849 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
110218849 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
110218849 (WNT2B)
05205 Proteoglycans in cancer
110218849 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
110218849 (WNT2B)
05226 Gastric cancer
110218849 (WNT2B)
05217 Basal cell carcinoma
110218849 (WNT2B)
05224 Breast cancer
110218849 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
110218849 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
110218849 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
110218849 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
110218849 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pcw00536
]
110218849 (WNT2B)
Glycosaminoglycan binding proteins [BR:
pcw00536
]
Heparan sulfate / Heparin
Morphogens
110218849 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
110218849
NCBI-ProteinID:
XP_020857499
UniProt:
A0A6P5LLV3
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All DBs
Position
Unknown
AA seq
398 aa
AA seq
DB search
MLSQGRTEEAPQLLRRRARLPVPAFAPAHRYPGRAAAPDGPGVPARLGLACLLLLLLTLP
PRIDASWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSLGEGARDWIRECQHQFRH
HRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTR
GRDRDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFL
KLECKCHGVSGSCTLRTCWHALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRH
ATRADLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSRGTDGCEVMCCGRGYDTTRVTRVT
QCECKFHWCCAVRCKECRDTVDVHTCKAPKKAEWLDQT
NT seq
1197 nt
NT seq
+upstream
nt +downstream
nt
atgctgagccagggcagaacggaggaagccccccagctcctccgtaggcgagcccggctc
cctgttcccgccttcgccccggcgcacagataccctggccgggcagcggcacccgacggt
cccggagtccctgcccgccttggcctcgcctgtctgttgctgctgttgcttacgctgccg
ccccgcatagatgcgtcctggtggtatatcggggcactgggggcccgggtgatctgtgac
aacatccccgggctggtgagccggcagcgccagttgtgccagcgctaccctgacatcatg
cgctccctgggtgagggggcccgggactggatccgcgagtgccagcaccagttccgtcat
caccgctggaactgcacaactctggaccgcgaccacaccgtctttggccgagttatgctc
agaagcagccgggaggcagcttttgtgtatgccatctcatcggcaggtgtggtccacgcc
atcacacgggcctgcagccagggtgagctcagtgtgtgcagctgtgacccttacacacgt
ggtcgggaccgagaccagcgtggagactttgactggggtggttgcagtgacaacatccat
tatggggtccgctttgccaaggcctttgtggatgctaaggagaagaggctgaaggatgcc
cgggccctcatgaacttgcacaacaatcgctgtggccgcacggctgtacgccgattccta
aagctggaatgtaagtgccatggagttagcggctcctgtaccctccgcacctgctggcat
gcactctcggacttccgccggactggtgactatctgcggaggcgctatgatggggctgtg
caggtgaccgccactcaggatggtgccaactttactgctgcccgtcagggctatcgccat
gccactcgggccgaccttgtctattttgacaactccccagactactgtgttctggacaag
gctgctgggtccctgggcactgcgggacgtgtatgcagtaagacgtctcgagggacagat
ggatgtgaggtcatgtgctgtggccgtggctatgacacaacccgagtcacacgtgtcacc
cagtgcgagtgcaaattccactggtgctgtgctgtccgctgtaaggagtgccgggacact
gtggatgtccacacctgcaaggcccccaagaaggcagaatggctggaccagacctga
DBGET
integrated database retrieval system