Trachypithecus francoisi (Francois's langur): 117072941
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Entry
117072941 CDS
T07225
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
tfn
Trachypithecus francoisi (Francois's langur)
Pathway
tfn04150
mTOR signaling pathway
tfn04310
Wnt signaling pathway
tfn04390
Hippo signaling pathway
tfn04550
Signaling pathways regulating pluripotency of stem cells
tfn04916
Melanogenesis
tfn04934
Cushing syndrome
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Alzheimer disease
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Pathways of neurodegeneration - multiple diseases
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Human papillomavirus infection
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Pathways in cancer
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Proteoglycans in cancer
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Basal cell carcinoma
tfn05224
Breast cancer
tfn05225
Hepatocellular carcinoma
tfn05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
tfn00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
117072941 (WNT2)
04390 Hippo signaling pathway
117072941 (WNT2)
04150 mTOR signaling pathway
117072941 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
117072941 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
117072941 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
117072941 (WNT2)
05205 Proteoglycans in cancer
117072941 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
117072941 (WNT2)
05226 Gastric cancer
117072941 (WNT2)
05217 Basal cell carcinoma
117072941 (WNT2)
05224 Breast cancer
117072941 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
117072941 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
117072941 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
117072941 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
117072941 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
tfn00536
]
117072941 (WNT2)
Glycosaminoglycan binding proteins [BR:
tfn00536
]
Heparan sulfate / Heparin
Morphogens
117072941 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
117072941
NCBI-ProteinID:
XP_033049320
LinkDB
All DBs
Position
Unknown
AA seq
360 aa
AA seq
DB search
MNAPLGGIWLWLPLLLTWLTPEVNSSWWYMRATGGSSRVMCDNVPGLVSSQRQLCHRHPD
VMRAISQGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVV
FAITRACSQGEVKSCSCDPKKMGSAKDSKGIFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG
AIQVVMNQDGTGFTVANERFKKPTKNDLVYFENSPDYCIRDREAGSLGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSHVTRMTKCGCKFHWCCAVRCQDCLEALDVHTCKAPKNADWTTPT
NT seq
1083 nt
NT seq
+upstream
nt +downstream
nt
atgaacgcccctctcggtggaatctggctctggctccctctgctcttgacctggctcacc
cccgaggtcaactcttcatggtggtacatgagagctacaggtggctcctccagggtgatg
tgcgataatgtgccaggcctggtgagcagccagcggcagctgtgtcaccgacatccagat
gtgatgcgtgccattagccagggcgtggccgagtggacagcggaatgccagcaccagttc
cgccagcaccgctggaattgcaacactctggacagggatcacagcctctttggcagggtc
ctactccgaagtagtcgggaatctgcctttgtttatgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaagtaaaatcttgttcctgtgatccaaag
aagatgggaagcgccaaggacagcaagggcatttttgattggggtggctgcagtgataac
attgactatgggatcaaatttgcccgtgcattcgtggatgccaaggaaaggaaaggaaag
gatgccagagccctgatgaatcttcataacaacagagctggcaggaaggctgtaaagcga
ttcttgaaacaagagtgcaaatgccatggggtgagcggctcgtgtactctaaggacatgc
tggctggccatggccgacttcaggaaaacgggcgattatctctggaggaagtacaatggg
gccatccaggtggtcatgaaccaggatggcacaggtttcactgtggctaacgagaggttt
aagaagccaacaaaaaatgacctcgtgtattttgagaattctccagactactgtatcagg
gaccgagaggcaggctccctgggtacagcaggccgagtgtgcaacctgacttcccggggc
atggacagctgcgaagtcatgtgctgtgggagaggctacgacacctcccatgtcacccgg
atgaccaagtgtggatgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg
gaggccctggacgtgcacacatgcaaggcccccaagaacgctgactggacaacccccaca
tga
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