KEGG   Panthera tigris altaica (Amur tiger): 102962277
Entry
102962277         CDS       T02988                                 
Symbol
WNT1
Name
(RefSeq) Wnt family member 1
  KO
K03209  wingless-type MMTV integration site family, member 1
Organism
ptg  Panthera tigris altaica (Amur tiger)
Pathway
ptg04150  mTOR signaling pathway
ptg04310  Wnt signaling pathway
ptg04390  Hippo signaling pathway
ptg04550  Signaling pathways regulating pluripotency of stem cells
ptg04916  Melanogenesis
ptg04934  Cushing syndrome
ptg05010  Alzheimer disease
ptg05022  Pathways of neurodegeneration - multiple diseases
ptg05165  Human papillomavirus infection
ptg05200  Pathways in cancer
ptg05205  Proteoglycans in cancer
ptg05207  Chemical carcinogenesis - receptor activation
ptg05217  Basal cell carcinoma
ptg05224  Breast cancer
ptg05225  Hepatocellular carcinoma
ptg05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ptg00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102962277 (WNT1)
   04390 Hippo signaling pathway
    102962277 (WNT1)
   04150 mTOR signaling pathway
    102962277 (WNT1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102962277 (WNT1)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102962277 (WNT1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102962277 (WNT1)
   05205 Proteoglycans in cancer
    102962277 (WNT1)
   05207 Chemical carcinogenesis - receptor activation
    102962277 (WNT1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102962277 (WNT1)
   05226 Gastric cancer
    102962277 (WNT1)
   05217 Basal cell carcinoma
    102962277 (WNT1)
   05224 Breast cancer
    102962277 (WNT1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102962277 (WNT1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102962277 (WNT1)
   05022 Pathways of neurodegeneration - multiple diseases
    102962277 (WNT1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102962277 (WNT1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ptg00536]
    102962277 (WNT1)
Glycosaminoglycan binding proteins [BR:ptg00536]
 Heparan sulfate / Heparin
  Morphogens
   102962277 (WNT1)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102962277
NCBI-ProteinID: XP_015400289
LinkDB
Position
Un
AA seq 232 aa
MSNPGPEGPAPTTHLTRGIVNVASSTNLLTDSKSLQLVLEPSLQLLSRKQRRLIRQNPGI
LHSVSGGLQSAVRECKWQFRNRRWNCPTATGPHLFGKIVNRGCRETAFIFAITSAGVTHS
VARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLFGREFVDSGEKGRDLRFLM
NLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLRAVGDVLRDRI
NT seq 699 nt   +upstreamnt  +downstreamnt
atgtcgaaccccgggcccgaaggccccgctcctaccacgcatctcaccaggggcatcgtg
aacgtagcctcctccacgaacctgctgaccgactccaagagtctacaactggtgctcgag
cccagtcttcagctgctgagccgcaaacagaggaggctgatccgccagaacccggggatc
ctgcacagcgtgagcggggggctgcagagcgctgtgcgagagtgcaagtggcagttccgc
aaccgccgctggaactgccccacggctacggggccccacctcttcggcaagatcgtcaac
cgaggctgtcgggaaacggcgtttattttcgctatcacctccgccggggttacccattcg
gtggcgcgctcctgctcagagggctccatcgagtcttgcacgtgcgactatcggcggcgc
ggccctgggggccccgattggcactgggggggctgcagcgacaacatcgacttcggccgc
ctcttcggcagggagtttgtggactccggggagaaggggcgggacctgcgcttcctcatg
aaccttcacaacaacgaggctggccgcacgactgtgttctctgagatgcgccaggagtgc
aagtgccacgggatgtcgggctcgtgcacggtgcgcacgtgctggatgcggctgcccacg
ctgcgcgccgtgggcgacgtgctgcgcgaccgaatctag

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