Vulpes vulpes (red fox): 112929869
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Entry
112929869 CDS
T05911
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
vvp
Vulpes vulpes (red fox)
Pathway
vvp04150
mTOR signaling pathway
vvp04310
Wnt signaling pathway
vvp04390
Hippo signaling pathway
vvp04550
Signaling pathways regulating pluripotency of stem cells
vvp04916
Melanogenesis
vvp04934
Cushing syndrome
vvp05010
Alzheimer disease
vvp05022
Pathways of neurodegeneration - multiple diseases
vvp05165
Human papillomavirus infection
vvp05200
Pathways in cancer
vvp05205
Proteoglycans in cancer
vvp05217
Basal cell carcinoma
vvp05224
Breast cancer
vvp05225
Hepatocellular carcinoma
vvp05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
vvp00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
112929869 (WNT2)
04390 Hippo signaling pathway
112929869 (WNT2)
04150 mTOR signaling pathway
112929869 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
112929869 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
112929869 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
112929869 (WNT2)
05205 Proteoglycans in cancer
112929869 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
112929869 (WNT2)
05226 Gastric cancer
112929869 (WNT2)
05217 Basal cell carcinoma
112929869 (WNT2)
05224 Breast cancer
112929869 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
112929869 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
112929869 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
112929869 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
112929869 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
vvp00536
]
112929869 (WNT2)
Glycosaminoglycan binding proteins [BR:
vvp00536
]
Heparan sulfate / Heparin
Morphogens
112929869 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
112929869
NCBI-ProteinID:
XP_025867930
UniProt:
A0A3Q7UKU0
LinkDB
All DBs
Position
Unknown
AA seq
360 aa
AA seq
DB search
MNAPVGGTGLWLPLLLAWLAPGVGASWWYMRATGGSSRVMCDNVPGLVSRQRQLCHRHPD
VMRAIGLGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAVSSAGVV
FAITRACSQGELKSCSCDPKKKGTAKDSKGSFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG
AIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDRDAGSPGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSRVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPTSADWAAPT
NT seq
1083 nt
NT seq
+upstream
nt +downstream
nt
atgaacgcccctgtcggtggaaccgggctctggctccccctgctcctggcctggctcgcc
cccggggtcggcgcctcgtggtggtacatgagagctacaggcggctcctccagggtgatg
tgtgacaatgtgccaggcctggtgagccgccagcgccagctgtgccaccgacacccggac
gtgatgcgtgccattggcctgggcgtggccgagtggacagcagagtgccagcaccagttc
cgccagcaccgctggaactgcaacacgctggacagggatcacagcctctttggcagggtc
ctgctccgaagtagtcgggaatctgcctttgtttacgccgtctcctcagctggagttgtg
tttgccatcaccagggcctgtagccaaggagagttaaaatcctgttcctgtgatccaaag
aagaagggaaccgccaaggacagcaagggcagtttcgactggggtggctgcagcgataac
attgactatgggatcaaatttgcccgagccttcgtggatgccaaggaaaggaagggaaag
gatgccagagccctgatgaaccttcacaacaacagagccggccggaaggcggtgaagcgg
ttcttgaagcaggaatgcaagtgtcacggcgtgagcggctcgtgtacgctgaggacatgc
tggctggccatggcggacttcagaaaaacgggcgattacctctggaggaagtacaacggg
gccatccaggtcgtcatgaaccaggatggcacggggttcacggtggctaacaagaggttc
aagaagccaaccaaaaatgacctcgtgtattttgagaattctccagactattgtatcagg
gaccgagacgcaggctccccggggacggcgggccgcgtgtgcaacctgacttcccgcggc
atggacagctgcgaggtcatgtgctgcgggagaggctacgacacgtcccgcgtcacgcgg
atgaccaagtgcgagtgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg
gaggccctagacgtgcacacatgcaaggcccccacgagcgccgactgggcggctcccaca
tga
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integrated database retrieval system