Rousettus aegyptiacus (Egyptian rousette): 107499803
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Entry
107499803 CDS
T06036
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b isoform X1
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
ray
Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04150
mTOR signaling pathway
ray04310
Wnt signaling pathway
ray04390
Hippo signaling pathway
ray04550
Signaling pathways regulating pluripotency of stem cells
ray04916
Melanogenesis
ray04934
Cushing syndrome
ray05010
Alzheimer disease
ray05022
Pathways of neurodegeneration - multiple diseases
ray05165
Human papillomavirus infection
ray05200
Pathways in cancer
ray05205
Proteoglycans in cancer
ray05217
Basal cell carcinoma
ray05224
Breast cancer
ray05225
Hepatocellular carcinoma
ray05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ray00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
107499803 (WNT2B)
04390 Hippo signaling pathway
107499803 (WNT2B)
04150 mTOR signaling pathway
107499803 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
107499803 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
107499803 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
107499803 (WNT2B)
05205 Proteoglycans in cancer
107499803 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
107499803 (WNT2B)
05226 Gastric cancer
107499803 (WNT2B)
05217 Basal cell carcinoma
107499803 (WNT2B)
05224 Breast cancer
107499803 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
107499803 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
107499803 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
107499803 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
107499803 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ray00536
]
107499803 (WNT2B)
Glycosaminoglycan binding proteins [BR:
ray00536
]
Heparan sulfate / Heparin
Morphogens
107499803 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
107499803
NCBI-ProteinID:
XP_015979803
LinkDB
All DBs
Position
Unknown
AA seq
402 aa
AA seq
DB search
MVGDHSITLSATAKLFLQNLWETVLPIRLRECGLRKGKGPYQGLMPNLSPSIPLLMQKKG
WDALTGPFPPCRYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQH
QFRHHRWNCTTVDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCD
PYTRGRHHDQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAV
RRFLKLECKCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQ
GYRRATRTDLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRV
TRVTQCECKFHWCCAVRCKECRNTVDIHTCKAPKKAEWLDQT
NT seq
1209 nt
NT seq
+upstream
nt +downstream
nt
atggtgggagaccactcaattactctctctgcaactgcaaaactatttctccagaacttg
tgggaaacggtcctacccatcaggctcagggaatgtgggttaaggaaggggaagggacca
taccaaggtctaatgccaaacctctccccttccattcctctcctaatgcagaagaagggc
tgggatgctctgacagggccatttcctccttgcaggtacatcggggcgctgggggcccga
gtgatctgtgacaacatccctggtctggtgagccggcagcggcagctgtgccagcgttat
ccagacatcatgcgctcggtgggcgagggtgcccgagaatggatccgagagtgtcagcac
cagttccgccaccaccgctggaactgcaccaccgtggaccgggaccacactgtctttggc
cgtgtcatgctcagaagtagccgggaagcagcatttgtgtacgccatctcgtcagcaggg
gtggtccatgctattactcgcgcctgcagccagggcgaactgagtgtgtgcagctgtgac
ccctacacccgtggccgacaccatgaccaacgtggggactttgactggggtggctgcagt
gataatatccactatggtgttcgctttgccaaggcctttgtggatgccaaggagaagagg
cttaaggatgcccgagccctcatgaacttacataacaaccgctgtggtcgcacggctgtg
cggcggtttctgaagctggagtgtaagtgccatggcgtgagtggctcctgtactctgcgc
acctgctggcgtgcactctcagacttccgccgcacaggtgattacctgcggcggcgctat
gatggggctgtgcaggtgacggccacccaggatggcgctaacttcacagcagcccgccaa
ggctatcgccgtgccacccgaactgaccttgtctactttgacaactccccagactactgt
gtcttggacaaggctgcaggttccctcggaactgcaggccgtgtctgcagcaagacatct
aaagggacagacggctgtgaaatcatgtgctgcggccgagggtatgacacaactcgagtc
acccgtgtcacccagtgtgagtgcaaattccactggtgctgtgcggtgcggtgcaaggag
tgcagaaatactgtggacatccatacttgcaaggcccccaagaaggcagagtggctggac
cagacctga
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