Pan paniscus (bonobo): 100990322
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Entry
100990322 CDS
T02283
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
pps
Pan paniscus (bonobo)
Pathway
pps04150
mTOR signaling pathway
pps04310
Wnt signaling pathway
pps04390
Hippo signaling pathway
pps04550
Signaling pathways regulating pluripotency of stem cells
pps04916
Melanogenesis
pps04934
Cushing syndrome
pps05010
Alzheimer disease
pps05022
Pathways of neurodegeneration - multiple diseases
pps05165
Human papillomavirus infection
pps05200
Pathways in cancer
pps05205
Proteoglycans in cancer
pps05217
Basal cell carcinoma
pps05224
Breast cancer
pps05225
Hepatocellular carcinoma
pps05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pps00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100990322 (WNT2)
04390 Hippo signaling pathway
100990322 (WNT2)
04150 mTOR signaling pathway
100990322 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100990322 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100990322 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100990322 (WNT2)
05205 Proteoglycans in cancer
100990322 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100990322 (WNT2)
05226 Gastric cancer
100990322 (WNT2)
05217 Basal cell carcinoma
100990322 (WNT2)
05224 Breast cancer
100990322 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100990322 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
100990322 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
100990322 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100990322 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pps00536
]
100990322 (WNT2)
Glycosaminoglycan binding proteins [BR:
pps00536
]
Heparan sulfate / Heparin
Morphogens
100990322 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100990322
NCBI-ProteinID:
XP_003808698
Ensembl:
ENSPPAG00000030407
UniProt:
A0A2R9AB51
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All DBs
Position
6:complement(154101025..154151405)
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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
gtgatgcgtgccattagccagggcgtggccgagtggacagcagaatgccagcaccagttc
cgccagcaccgctggaattgcaacaccctggacagggatcacagcctctttggcagggtc
ctactccgaagtagtcgggaatctgcctttgtttatgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaagtaaaatcctgttcctgtgatccaaag
aagatgggaagcgccaaggacagcaaaggcatttttgattggggtggctgcagtgataac
attgactatggaatcaaatttgcccgcgcatttgtggatgcaaaggaaaggaaaggaaag
gatgccagagccctgatgaatcttcacaacaacagagctggcaggaaggctgtaaagcgg
ttcttgaaacaagagtgcaagtgccacggggtgagcggctcatgtactctcaggacatgc
tggctggccatggccgacttcaggaaaacgggcgattatctctggaggaagtacaatggg
gccatccaggtggtcatgaaccaggatggcacaggtttcactgtggctaacgagaggttt
aagaagccaacaaaaaatgacctcgtgtattttgagaattctccagactactgtatcagg
gaccgagaagcaggctccctgggtacagcaggccgtgtgtgcaacctgacttcccggggc
atggacagctgtgaagtcatgtgctgtgggagaggctacgacacctcccatgtcacccgg
atgaccaagtgtgggtgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg
gaagctctggatgtgcacacatgcaaggcccccaagaacgctgactggacaacccctaca
tga
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