Lynx rufus (bobcat): 124500979
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Entry
124500979 CDS
T08475
Name
(RefSeq) protein Wnt-10b
KO
K01357
wingless-type MMTV integration site family, member 10
Organism
lruf
Lynx rufus (bobcat)
Pathway
lruf04150
mTOR signaling pathway
lruf04310
Wnt signaling pathway
lruf04390
Hippo signaling pathway
lruf04519
Cadherin signaling
lruf04550
Signaling pathways regulating pluripotency of stem cells
lruf04916
Melanogenesis
lruf04934
Cushing syndrome
lruf05010
Alzheimer disease
lruf05022
Pathways of neurodegeneration - multiple diseases
lruf05165
Human papillomavirus infection
lruf05200
Pathways in cancer
lruf05205
Proteoglycans in cancer
lruf05217
Basal cell carcinoma
lruf05224
Breast cancer
lruf05225
Hepatocellular carcinoma
lruf05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
lruf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
124500979
04390 Hippo signaling pathway
124500979
04150 mTOR signaling pathway
124500979
09133 Signaling molecules and interaction
04519 Cadherin signaling
124500979
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
124500979
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
124500979
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
124500979
05205 Proteoglycans in cancer
124500979
09162 Cancer: specific types
05225 Hepatocellular carcinoma
124500979
05226 Gastric cancer
124500979
05217 Basal cell carcinoma
124500979
05224 Breast cancer
124500979
09172 Infectious disease: viral
05165 Human papillomavirus infection
124500979
09164 Neurodegenerative disease
05010 Alzheimer disease
124500979
05022 Pathways of neurodegeneration - multiple diseases
124500979
09167 Endocrine and metabolic disease
04934 Cushing syndrome
124500979
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
lruf00536
]
124500979
Glycosaminoglycan binding proteins [BR:
lruf00536
]
Heparan sulfate / Heparin
Morphogens
124500979
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
124500979
NCBI-ProteinID:
XP_046920812
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
atgccggaggagccccggccgcggcctccgccctcgggcttcgcgggtctcctgttcctg
gcgttgtgcagtcgggccctcagcaatgagattctgggcctgaagctgcccggcgagccg
ccgctgaccgccaacaccgtatgcttgacgctgtcgggcctgagcaaacggcagctaggc
ctgtgcctgcgcagccccgacgtgacggcatccgcgcttcagggcctgcatatcgcggtc
cacgagtgtcagcaccagctgcgcgaccagcgctggaactgctcggcgctggagggcggc
ggccgcctgccgcaccacagcgccatcctcaagcgcggtttccgggagagtgctttttcc
ttctccatgctggctgcaggggtcatgcacgcggtagccacggcctgcagcctgggcaag
ctggtgagctgcggctgcggctggaagggcagtggtgagcaggatcggctgagggccaaa
ctactgcagctgcaggcactgtcccggggcaagagtttcccccactccctgcccagtcct
ggccccggctcaggccccagccctggcccccaggacacatgggaatggggtggctgtaac
catgacatggactttggagagaagttctctcgggatttcttggattccagggaagctccc
cgggacatccaggcaagaatgcgaatccacaacaacagggtggggcgacaggtggtgact
gaaaacctgaagcggaaatgcaagtgccatggcacgtcgggcagttgccagttcaagacc
tgctggagggcggccccagaattccgggcagtgggggcggcgttgagggagcggctgggt
cgggccatcttcatcgatacccacaaccgcaactccggagccttccagccccgcctgcgt
ccccgtcgcctctcaggagagctggtctactttgagaagtcgcctgacttctgtgagcga
gaccctgccgtgggctccccgggcactcggggccgggcctgcaataagaccagccgcctg
ctggatggctgtggcagcctgtgctgtggccgtgggcacaacctgctccggcagacacga
gtcgagcgctgtcattgccgcttccactggtgctgctacgtgctgtgtgatgagtgcaag
gtcacagagtgggtcaacgtgtgtaagtga
DBGET
integrated database retrieval system