Macaca mulatta (rhesus monkey): 704991
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Entry
704991 CDS
T01028
Symbol
WNT2
Name
(RefSeq) protein Wnt-2 precursor
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc04150
mTOR signaling pathway
mcc04310
Wnt signaling pathway
mcc04390
Hippo signaling pathway
mcc04550
Signaling pathways regulating pluripotency of stem cells
mcc04916
Melanogenesis
mcc04934
Cushing syndrome
mcc05010
Alzheimer disease
mcc05022
Pathways of neurodegeneration - multiple diseases
mcc05165
Human papillomavirus infection
mcc05200
Pathways in cancer
mcc05205
Proteoglycans in cancer
mcc05217
Basal cell carcinoma
mcc05224
Breast cancer
mcc05225
Hepatocellular carcinoma
mcc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
704991 (WNT2)
04390 Hippo signaling pathway
704991 (WNT2)
04150 mTOR signaling pathway
704991 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
704991 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
704991 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
704991 (WNT2)
05205 Proteoglycans in cancer
704991 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
704991 (WNT2)
05226 Gastric cancer
704991 (WNT2)
05217 Basal cell carcinoma
704991 (WNT2)
05224 Breast cancer
704991 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
704991 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
704991 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
704991 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
704991 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mcc00536
]
704991 (WNT2)
Glycosaminoglycan binding proteins [BR:
mcc00536
]
Heparan sulfate / Heparin
Morphogens
704991 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
704991
NCBI-ProteinID:
NP_001162158
Ensembl:
ENSMMUG00000047811
UniProt:
F7E738
A0A8J8XPN3
LinkDB
All DBs
Position
3:complement(143484064..143530116)
Genome browser
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
cgccagcaccgctggaattgcaacaccctggacagggatcacagcctctttggcagggtc
ctactccgaagtagtcgggaatctgcctttgtttatgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaagtaaaatcctgttcctgtgatccaaag
aagatgggaagcgccaaggacagcaagggcatttttgattggggtggctgcagtgataac
attgactatgggatcaaatttgcccgcgcattcgtggatgccaaggaaaggaaaggaaag
gatgccagagccctgatgaatcttcataacaacagagctggcaggaaggctgtaaagcgg
ttcttgaaacaagagtgcaaatgccatggggtgagcggctcgtgtactctcaggacatgc
tggctggccatggccgacttcaggaaaacgggcgattatctctggaggaagtacaatggg
gccatccaggtggtcatgaaccaggatggtacaggtttcactgtggctaacgagaggttt
aagaagccaacaaaaaatgacctcgtgtattttgagaattctccagactactgtatcagg
gaccgagaggcaggctccctgggtacagcaggccgtgtgtgcaacctgacttcccggggc
atggacagctgcgaagtcatgtgctgtgggagaggctacgacacctcccatgtcacccgg
atgaccaagtgtgggtgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg
gaggccctggatgtgcacacatgcaaggcccccaagaacgctgactggacaacccccaca
tga
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