Panthera pardus (leopard): 109248384
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Entry
109248384 CDS
T06062
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
ppad
Panthera pardus (leopard)
Pathway
ppad04150
mTOR signaling pathway
ppad04310
Wnt signaling pathway
ppad04390
Hippo signaling pathway
ppad04550
Signaling pathways regulating pluripotency of stem cells
ppad04916
Melanogenesis
ppad04934
Cushing syndrome
ppad05010
Alzheimer disease
ppad05022
Pathways of neurodegeneration - multiple diseases
ppad05165
Human papillomavirus infection
ppad05200
Pathways in cancer
ppad05205
Proteoglycans in cancer
ppad05217
Basal cell carcinoma
ppad05224
Breast cancer
ppad05225
Hepatocellular carcinoma
ppad05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ppad00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
109248384 (WNT2)
04390 Hippo signaling pathway
109248384 (WNT2)
04150 mTOR signaling pathway
109248384 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
109248384 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
109248384 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
109248384 (WNT2)
05205 Proteoglycans in cancer
109248384 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
109248384 (WNT2)
05226 Gastric cancer
109248384 (WNT2)
05217 Basal cell carcinoma
109248384 (WNT2)
05224 Breast cancer
109248384 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
109248384 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
109248384 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
109248384 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
109248384 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ppad00536
]
109248384 (WNT2)
Glycosaminoglycan binding proteins [BR:
ppad00536
]
Heparan sulfate / Heparin
Morphogens
109248384 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
109248384
NCBI-ProteinID:
XP_019273585
Ensembl:
ENSPPRG00000005517
UniProt:
A0A9V1E3X5
LinkDB
All DBs
Position
Unknown
AA seq
360 aa
AA seq
DB search
MNAPLGGIWPWLPLLLTWLTPEVSSSWWYMRATGGSSRVMCDNVPGLVSRQRQLCHRHPD
VMRAIGLGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAVSSAGVV
FAITRACSQGELKSCSCDPKKKGTAKDSKGNFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG
AIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDRDAGSLGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSHVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPKSVDWAAPT
NT seq
1083 nt
NT seq
+upstream
nt +downstream
nt
atgaacgcccctctcggtggaatctggccctggctccccctgctcttgacctggctcacc
cctgaggtcagctcttcatggtggtacatgagagctacaggtggctcctccagggtgatg
tgtgacaatgtgccaggcctggtgagccgccagcggcagctgtgccaccgacacccagat
gtgatgcgtgccattggcctaggcgtggccgagtggactgcagagtgtcagcaccaattc
cgccagcaccgctggaactgcaacaccctcgacagagatcacagcctcttcggcagggtc
ctgctccgaagtagtcgggaatctgcctttgtttacgccgtctcctcagcgggagttgtg
tttgccatcaccagggcctgtagccaaggagaattaaaatcctgttcctgtgatccaaag
aagaagggaaccgccaaggacagcaagggaaatttcgactggggtggctgcagtgataac
attgactatgggatcaaatttgcccgagcatttgtggatgccaaggaaaggaaaggaaag
gatgccagagccctgatgaaccttcacaacaacagagccggcaggaaggcggtaaagcgg
ttcttgaaacaagaatgcaagtgtcacggagtgagtggctcgtgtactctgaggacatgc
tggctggccatggctgacttcagaaaaacgggcgattacctctggaggaagtacaacggg
gccatccaggtcgtcatgaaccaggatggcactggtttcactgtggctaacaagaggttt
aagaagccaacaaaaaatgacctcgtgtattttgagaattctccagactattgtatcagg
gaccgagatgcaggatctctgggtacagcaggccgtgtatgcaacctgacttcccggggc
atggacagctgcgaggttatgtgctgcgggagaggctatgacacctcccacgtcacccgg
atgaccaagtgcgagtgtaagttccactggtgctgtgccgtgcgctgtcaggactgtctg
gaggccctggacgtgcacacatgcaaggcccctaaaagcgttgactgggcggctcccaca
tga
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integrated database retrieval system