Panthera pardus (leopard): 109267221
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Entry
109267221 CDS
T06062
Symbol
WNT11
Name
(RefSeq) protein Wnt-11
KO
K01384
wingless-type MMTV integration site family, member 11
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
109267221 (WNT11)
04390 Hippo signaling pathway
109267221 (WNT11)
04150 mTOR signaling pathway
109267221 (WNT11)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
109267221 (WNT11)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
109267221 (WNT11)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
109267221 (WNT11)
05205 Proteoglycans in cancer
109267221 (WNT11)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
109267221 (WNT11)
05226 Gastric cancer
109267221 (WNT11)
05217 Basal cell carcinoma
109267221 (WNT11)
05224 Breast cancer
109267221 (WNT11)
09172 Infectious disease: viral
05165 Human papillomavirus infection
109267221 (WNT11)
09164 Neurodegenerative disease
05010 Alzheimer disease
109267221 (WNT11)
05022 Pathways of neurodegeneration - multiple diseases
109267221 (WNT11)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
109267221 (WNT11)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ppad00536
]
109267221 (WNT11)
Glycosaminoglycan binding proteins [BR:
ppad00536
]
Heparan sulfate / Heparin
Morphogens
109267221 (WNT11)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
109267221
NCBI-ProteinID:
XP_019305415
Ensembl:
ENSPPRG00000006331
UniProt:
A0A9V1FM64
LinkDB
All DBs
Position
Unknown
AA seq
354 aa
AA seq
DB search
MRARPRVCEALLFALALQTGVCYGIKWLALSKTPAALALNQTQHCKQLEGLVSAQVQLCR
SNLELMHTIVHAAREVMKACRRAFADMRWNCSSIELAPNYLLDLERGTRESAFVYALSAA
AISHAIARACTSGDLPGCSCGPVPGEPPGPGNRWGGCADNLSYGLLMGAKFSDAPMKVKK
TGSQANKLMRLHNSEVGRQALRASLEMKCKCHGVSGSCSIRTCWKGLQELRDVASDLKTR
YLSATKVVHRPMGTRKHLVPKDLDIRPVKDSELVYLQSSPDFCMKNEKVGSHGTQDRQCN
KTSHGSDSCDLMCCGRGYNPYTDRVVERCHCKYHWCCYVTCRRCERTVERYVCK
NT seq
1065 nt
NT seq
+upstream
nt +downstream
nt
atgagggcgcggccgcgagtctgcgaggcgctgctcttcgccctggcgctccagaccggc
gtgtgctacggcatcaaatggctggcgctgtccaagaccccggcggccctcgcgctgaac
cagacgcagcactgcaagcagctggaggggttggtatctgcgcaggtgcagctgtgccgc
agtaacctggagctcatgcacaccatcgtgcacgccgcccgcgaggtcatgaaggcctgc
cgcagggccttcgcggacatgcgctggaactgctcctccatcgagcttgcccccaactac
ctgcttgacctggagagagggacccgggagtcagccttcgtgtatgcgctgtcggcggcc
gccatcagccacgccatcgcccgggcctgcacctccggcgacctgcccggctgctcctgc
ggccctgtcccaggtgagccacccgggcccgggaaccgctggggaggatgtgcggacaac
ctcagctacgggctcctcatgggggccaagttttccgatgctcctatgaaggtgaaaaaa
acaggatcccaagccaataaactgatgcgtctacacaacagtgaagtggggagacaggct
ctgcgcgcctctctggaaatgaagtgtaagtgccacggggtatctggctcctgctccatc
cgcacctgctggaaggggctgcaggagcttcgggatgtggcctctgacctcaagacccgc
tacctgtcggccaccaaggtggtgcaccgacccatgggcacccgcaagcacctggtgccc
aaggacctggatatcaggcctgtgaaggactcggagcttgtctatctgcagagctcgccc
gacttctgcatgaagaacgagaaggtgggctcccatgggacgcaagacaggcagtgcaac
aagacgtcccacggcagtgacagctgtgacctcatgtgctgcggacgcggctacaacccc
tacacggaccgcgtggtcgagcggtgccactgcaaataccattggtgctgctacgtcacc
tgccgtaggtgcgagcgcaccgtggagcgctatgtctgcaagtga
DBGET
integrated database retrieval system