Myotis yumanensis (Yuma myotis): 139016130
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Entry
139016130 CDS
T10762
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
myum Myotis yumanensis (Yuma myotis)
Pathway
myum04150
mTOR signaling pathway
myum04310
Wnt signaling pathway
myum04390
Hippo signaling pathway
myum04550
Signaling pathways regulating pluripotency of stem cells
myum04916
Melanogenesis
myum04934
Cushing syndrome
myum05010
Alzheimer disease
myum05022
Pathways of neurodegeneration - multiple diseases
myum05165
Human papillomavirus infection
myum05200
Pathways in cancer
myum05205
Proteoglycans in cancer
myum05217
Basal cell carcinoma
myum05224
Breast cancer
myum05225
Hepatocellular carcinoma
myum05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
myum00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
139016130 (WNT2)
04390 Hippo signaling pathway
139016130 (WNT2)
04150 mTOR signaling pathway
139016130 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
139016130 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
139016130 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
139016130 (WNT2)
05205 Proteoglycans in cancer
139016130 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
139016130 (WNT2)
05226 Gastric cancer
139016130 (WNT2)
05217 Basal cell carcinoma
139016130 (WNT2)
05224 Breast cancer
139016130 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
139016130 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
139016130 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
139016130 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
139016130 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
myum00536
]
139016130 (WNT2)
Glycosaminoglycan binding proteins [BR:
myum00536
]
Heparan sulfate / Heparin
Morphogens
139016130 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
139016130
NCBI-ProteinID:
XP_070279874
LinkDB
All DBs
Position
Unknown
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
tgtgacaatgtgccaggcctggtgagccgccagcggcagctgtgccaccgacacccggac
gtgatgcgtgccattggcctgggcgtggcagagtggacaacggagtgccagcaccaattc
cgccagcaccgctggaactgcaacaccctggacagggaccacagcctcttcggcagggtc
ctgctccgaagtagtcgggaatctgcctttgtttacgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaattaaaatcctgttcctgtgatccaaag
aagaagggcagttccaaggacaccaggggcaccttcgactggggcggctgcagtgataac
attgactatgggatcaagtttgcccgtgcgtttgtggatgccaaggagcggaaaggcaag
gacgccagagccctgatgaacctgcacaacaacagggccggcaggaaggctgtgaagcgg
ttcttgaagcaagagtgcaagtgccacggcgtgagcggttcctgcacgctgaggacgtgc
tggctggccatggccgacttcaggaggacgggcgactacctgtggaagaagtacaacggg
gccatccaggtggtcatgaaccaggacggcactggcttcactgtggctaacaagaggttt
aagaagccaacgaaaaatgacctcgtgtattttgagaattctccagactactgtatcagg
gaccgagatgcaggctccctgggcacggccggccgcgtgtgcaacctgacctcccggggc
atggacagctgcgaagtcatgtgctgcggcagaggctacgacacgtcccgcgtcacgcgg
atgaccaagtgcgagtgcaagttccactggtgctgtgccgtgcgctgccaggactgcctg
gaggccctggatgtgcacacgtgcaaggccccgaagagcgccgactgggcggcgcctaca
tga
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