Myotis brandtii (Brandt's bat): 102261227
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Entry
102261227 CDS
T02920
Symbol
WNT2
Name
(RefSeq) Wnt family member 2
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
myb
Myotis brandtii (Brandt's bat)
Pathway
myb04150
mTOR signaling pathway
myb04310
Wnt signaling pathway
myb04390
Hippo signaling pathway
myb04550
Signaling pathways regulating pluripotency of stem cells
myb04916
Melanogenesis
myb04934
Cushing syndrome
myb05010
Alzheimer disease
myb05022
Pathways of neurodegeneration - multiple diseases
myb05165
Human papillomavirus infection
myb05200
Pathways in cancer
myb05205
Proteoglycans in cancer
myb05217
Basal cell carcinoma
myb05224
Breast cancer
myb05225
Hepatocellular carcinoma
myb05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
myb00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102261227 (WNT2)
04390 Hippo signaling pathway
102261227 (WNT2)
04150 mTOR signaling pathway
102261227 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102261227 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102261227 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102261227 (WNT2)
05205 Proteoglycans in cancer
102261227 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102261227 (WNT2)
05226 Gastric cancer
102261227 (WNT2)
05217 Basal cell carcinoma
102261227 (WNT2)
05224 Breast cancer
102261227 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102261227 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
102261227 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
102261227 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102261227 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
myb00536
]
102261227 (WNT2)
Glycosaminoglycan binding proteins [BR:
myb00536
]
Heparan sulfate / Heparin
Morphogens
102261227 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
102261227
NCBI-ProteinID:
XP_005877754
LinkDB
All DBs
Position
Un
AA seq
360 aa
AA seq
DB search
MNGPLGGIWLWLPLLLTWLRPEVSSSWWYMRATGGASRVMCDNVPGLVSRQRQLCHRHPD
VMRAIGLGVAEWTTECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVV
FAITRACSQGELKSCSCDPKKKGSSKDTRGTFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRRTGDYLWKKYNG
AIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDRDAGSLGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSRVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPKSADWAAPT
NT seq
1083 nt
NT seq
+upstream
nt +downstream
nt
atgaacggccctctcggtggaatctggctctggctccctctgctcttgacctggctcagg
cctgaggtcagctcttcatggtggtacatgagagctacaggcggcgcctccagggtgatg
tgtgacaatgtgccaggcctggtgagccgccagcggcagctgtgccaccgacacccggat
gtgatgcgtgccattggcctgggcgtggcagagtggacaacggagtgccagcaccaattc
cgccagcaccgctggaactgcaacaccctggacagggaccacagcctcttcggcagggtc
ctgctccgaagtagtcgggaatctgcctttgtttacgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaattaaaatcctgttcctgtgatccaaag
aagaagggcagttccaaggacaccaggggcaccttcgactggggcggctgcagtgataac
attgactatgggatcaagtttgcccgcgcgtttgtggatgccaaggagcggaaaggcaag
gacgccagagccctgatgaacctgcacaacaacagggccggcaggaaggctgtgaagcgg
ttcttgaagcaagagtgcaagtgccacggtgtgagcggttcctgtacgctgaggacgtgc
tggctggccatggccgacttcaggaggacgggcgactacctgtggaagaagtacaacggg
gccatccaggtggtcatgaaccaggacggcactggcttcactgtggccaacaagaggttt
aagaagccaacgaaaaatgacctcgtgtattttgagaattctccagactactgtatcagg
gaccgagatgcaggctccctgggcacggccggccgtgtgtgcaacctgacctcccggggc
atggacagctgcgaagtcatgtgctgcggcagaggctacgacacgtcccgcgtcacgcgg
atgaccaagtgcgagtgcaagttccactggtgctgtgccgtgcgctgccaggactgcctg
gaggccctggacgtgcacacgtgcaaggccccgaagagcgccgattgggcggcacccaca
tga
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integrated database retrieval system