Panthera pardus (leopard): 109249054
Help
Entry
109249054 CDS
T06062
Symbol
WNT10B
Name
(RefSeq) protein Wnt-10b
KO
K01357
wingless-type MMTV integration site family, member 10
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
109249054 (WNT10B)
04390 Hippo signaling pathway
109249054 (WNT10B)
04150 mTOR signaling pathway
109249054 (WNT10B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
109249054 (WNT10B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
109249054 (WNT10B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
109249054 (WNT10B)
05205 Proteoglycans in cancer
109249054 (WNT10B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
109249054 (WNT10B)
05226 Gastric cancer
109249054 (WNT10B)
05217 Basal cell carcinoma
109249054 (WNT10B)
05224 Breast cancer
109249054 (WNT10B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
109249054 (WNT10B)
09164 Neurodegenerative disease
05010 Alzheimer disease
109249054 (WNT10B)
05022 Pathways of neurodegeneration - multiple diseases
109249054 (WNT10B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
109249054 (WNT10B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ppad00536
]
109249054 (WNT10B)
Glycosaminoglycan binding proteins [BR:
ppad00536
]
Heparan sulfate / Heparin
Morphogens
109249054 (WNT10B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
109249054
NCBI-ProteinID:
XP_019274764
Ensembl:
ENSPPRG00000011632
UniProt:
A0A9V1E5U9
LinkDB
All DBs
Position
Unknown
AA seq
389 aa
AA seq
DB search
MPEEPRPRPPPSGFAGLLFLALCSRALSNEILGLKLPGEPPLTANTVCLTLSGLSKRQLG
LCLRSPDVTASALQGLHIAVHECQHQLRDQRWNCSALEGGGRLPHHSAILKRGFRESAFS
FSMLAAGVMHAVATACSLGKLVSCGCGWKGSGEQDRLRAKLLQLQALSRGKSFPHSLPSP
GPGSGPSPGPQDTWEWGGCNHDMDFGEKFSRDFLDSREAPRDIQARMRIHNNRVGRQVVT
ENLKRKCKCHGTSGSCQFKTCWRAAPEFRAVGAALRERLGRAIFIDTHNRNSGAFQPRLR
PRRLSGELVYFEKSPDFCERDPAVGSPGTRGRACNKTSRLLDGCGSLCCGRGHNLLRQTR
VERCHCRFHWCCYVLCDECKVTEWVNVCK
NT seq
1170 nt
NT seq
+upstream
nt +downstream
nt
atgccggaggagccccggccgcgccctccgccctcgggcttcgcgggtctcctgtttctg
gcgttgtgcagtcgggccctcagcaatgagattctgggcctgaagctgcccggcgagccg
ccgctgaccgccaacaccgtatgcttgacgctgtcgggcctgagcaaacggcagctaggc
ctgtgcctgcgcagccccgacgtgacggcatccgcgcttcagggcctgcatatcgcggtc
cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctcggcgctggagggcggc
ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgggagagtgctttttcc
ttctccatgctggctgcaggggtcatgcacgcggtagccacggcctgcagcctgggcaag
ctggtgagctgcggctgcggctggaagggcagtggtgagcaggatcggctgagggccaaa
ctactgcagctgcaggcactgtcccggggcaagagtttcccccactccctgcccagtcct
ggccctggctcaggccccagccctggcccccaggacacatgggaatggggtggctgtaac
catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc
cgggacatccaggcaagaatgcgaatccacaacaacagggtggggcgacaggtggtgact
gaaaacctgaagcggaaatgcaagtgccatggcacgtcaggcagttgccagttcaagacc
tgctggagggcggccccagagttccgggcagtgggggcggcgttgagggagcggctgggt
cgggccatcttcatcgatacccacaaccgcaactccggagccttccagccccgcctgcgt
ccccgtcgcctctcaggagagctggtctactttgagaagtcgcctgacttctgtgagcga
gaccctgccgtgggctccccgggcactcggggccgggcctgcaataagaccagccgcctg
ctggatggctgtggcagcctgtgctgtggccgtgggcacaacctgctccggcagacacga
gtcgagcgctgtcattgccgcttccactggtgctgctacgtgctgtgtgatgagtgcaag
gtcacagagtgggtcaacgtgtgtaagtga
DBGET
integrated database retrieval system