Vicugna pacos (alpaca): 102525166
Help
Entry
102525166 CDS
T08098
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
vpc
Vicugna pacos (alpaca)
Pathway
vpc04150
mTOR signaling pathway
vpc04310
Wnt signaling pathway
vpc04390
Hippo signaling pathway
vpc04550
Signaling pathways regulating pluripotency of stem cells
vpc04916
Melanogenesis
vpc04934
Cushing syndrome
vpc05010
Alzheimer disease
vpc05022
Pathways of neurodegeneration - multiple diseases
vpc05165
Human papillomavirus infection
vpc05200
Pathways in cancer
vpc05205
Proteoglycans in cancer
vpc05217
Basal cell carcinoma
vpc05224
Breast cancer
vpc05225
Hepatocellular carcinoma
vpc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
vpc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102525166 (WNT2B)
04390 Hippo signaling pathway
102525166 (WNT2B)
04150 mTOR signaling pathway
102525166 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102525166 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102525166 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102525166 (WNT2B)
05205 Proteoglycans in cancer
102525166 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102525166 (WNT2B)
05226 Gastric cancer
102525166 (WNT2B)
05217 Basal cell carcinoma
102525166 (WNT2B)
05224 Breast cancer
102525166 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102525166 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
102525166 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
102525166 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102525166 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
vpc00536
]
102525166 (WNT2B)
Glycosaminoglycan binding proteins [BR:
vpc00536
]
Heparan sulfate / Heparin
Morphogens
102525166 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
102525166
NCBI-ProteinID:
XP_015106329
UniProt:
A0A6J0AZD5
LinkDB
All DBs
Position
9
AA seq
299 aa
AA seq
DB search
MRSVGEGAREWIRECQHQFRHHRWNCTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVH
AITRACSQGELSVCSCDPYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKD
ARALMNLHNNRCGRTAVRRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGA
VQVTATQDGVNFTAARQGYRRATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGT
DGCEIMCCGRGYDTTRVTRVTQCECKFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
900 nt
NT seq
+upstream
nt +downstream
nt
atgcgctcggtgggtgagggtgcccgagaatggatccgagagtgtcagcaccagttccgc
caccaccgctggaactgcaccacgctggaccgggaccacactgtcttcggccgagtcatg
ctcagaagtagccgggaggcagcatttgtatatgccatctcttcagcaggagtggtccac
gctatcactcgggcctgtagccagggtgagctgagtgtgtgcagctgtgacccctatacc
cgtggccgacaccatgaccaacgtggggactttgactggggtggttgcagtgacaacatt
cactatggtgttcgctttgccaaggccttcgtggatgccaaggagaagaggcttaaggat
gcccgggctctcatgaacttacataacaaccgctgtggtcgcacggctgtgcggcggttt
ctgaagctggaatgtaagtgccacggcgtgagtggctcctgtactctgcgcacctgctgg
cgtgctctctcagacttccgccgcacaggtgattacctgcggcgacgctatgacggggcc
gtgcaggtgacggccacccaggatggtgtcaacttcacagcagcccgccaaggctatcgc
cgtgccacccggactgaccttgtctactttgacaactccccagactactgtgttttggac
aaggctgcaggttccctaggcactgcaggccgtgtctgcagcaagacatctaaagggaca
gatggttgtgaaatcatgtgctgcggccgagggtatgacacaactcgagttacccgcgtc
acccagtgtgagtgcaaattccactggtgctgtgctgtgcgctgcaaggagtgcagaaac
actgtggacgtccatacttgcaaggcccccaagaaggcagagtggctggatcagacctga
DBGET
integrated database retrieval system