KEGG   Vulpes lagopus (Arctic fox): 121480178
Entry
121480178         CDS       T07435                                 
Symbol
WNT1
Name
(RefSeq) proto-oncogene Wnt-1 isoform X1
  KO
K03209  wingless-type MMTV integration site family, member 1
Organism
vlg  Vulpes lagopus (Arctic fox)
Pathway
vlg04150  mTOR signaling pathway
vlg04310  Wnt signaling pathway
vlg04390  Hippo signaling pathway
vlg04550  Signaling pathways regulating pluripotency of stem cells
vlg04916  Melanogenesis
vlg04934  Cushing syndrome
vlg05010  Alzheimer disease
vlg05022  Pathways of neurodegeneration - multiple diseases
vlg05165  Human papillomavirus infection
vlg05200  Pathways in cancer
vlg05205  Proteoglycans in cancer
vlg05207  Chemical carcinogenesis - receptor activation
vlg05217  Basal cell carcinoma
vlg05224  Breast cancer
vlg05225  Hepatocellular carcinoma
vlg05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:vlg00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    121480178 (WNT1)
   04390 Hippo signaling pathway
    121480178 (WNT1)
   04150 mTOR signaling pathway
    121480178 (WNT1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    121480178 (WNT1)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    121480178 (WNT1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    121480178 (WNT1)
   05205 Proteoglycans in cancer
    121480178 (WNT1)
   05207 Chemical carcinogenesis - receptor activation
    121480178 (WNT1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    121480178 (WNT1)
   05226 Gastric cancer
    121480178 (WNT1)
   05217 Basal cell carcinoma
    121480178 (WNT1)
   05224 Breast cancer
    121480178 (WNT1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    121480178 (WNT1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    121480178 (WNT1)
   05022 Pathways of neurodegeneration - multiple diseases
    121480178 (WNT1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    121480178 (WNT1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:vlg00536]
    121480178 (WNT1)
Glycosaminoglycan binding proteins [BR:vlg00536]
 Heparan sulfate / Heparin
  Morphogens
   121480178 (WNT1)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 121480178
NCBI-ProteinID: XP_041592455
LinkDB
Position
21:40083005..40086934
AA seq 370 aa
MGHWALLPGGVSAALLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS
LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTASGPHLFGKIVNRG
CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF
GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR
AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT
YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC
THTRVLHECL
NT seq 1113 nt   +upstreamnt  +downstreamnt
atggggcactgggcgctgctgcccggcggggtttctgctgcgctcttgctggcgctggcc
gctctgcccgcagccctggccgccaacagcagcggccgatggtggggcatcgtgaacgtc
gcctcctccacgaacctgctgaccgactccaagagtctgcaactggtgctggagcccagt
cttcagctgctgagccgcaaacagcggaggctgatccgtcagaacccggggatcctgcac
agcgtgagcggggggctgcagagcgctgtgcgagagtgcaagtggcagttccgcaaccgc
cgctggaactgccccacggcttcggggccccacctcttcggcaagatcgtcaaccgaggc
tgtcgggaaaccgcatttatcttcgccatcacctccgccggggttacccactcagtggca
cgctcctgctcagagggctccatcgagtcctgcacgtgcgactaccggcggcgcggcccc
gggggccccgactggcactgggggggctgcagcgacaacatcgacttcggccgcctcttc
ggcagggagtttgtggactccggggagaaggggcgggacctgcgcttcctcatgaacctg
cacaacaacgaggcgggccgcacgacggtgttctccgagatgcgccaggagtgcaagtgc
cacgggatgtcgggctcgtgcacggtgcgcacgtgctggatgcggctgcccacgctgcgc
gccgtgggcgacgtgctgcgcgaccgcttcgatggggcctcgcgcgtcctctacggcaac
cgcggcagcaaccgagcctcccgggcggagctgctgcgcctggagcccgaagaccccgcg
cacaagccgccctccccccacgacctcgtctactttgagaaatcgcccaatttctgcacc
tacagcggacgcctggggacggcgggcacggcggggcgcgcctgcaacagctcctcgccc
gcgctggacggctgcgagctgctctgctgcggccggggccaccgcacgcgcacacagcgc
gtcaccgagcgctgcaactgcaccttccactggtgctgccacgtcagctgccgcaactgc
acgcacacgcgcgtactgcacgagtgtctgtga

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