KEGG   Vicugna pacos (alpaca): 102535386
Entry
102535386         CDS       T08098                                 
Symbol
WNT1
Name
(RefSeq) proto-oncogene Wnt-1
  KO
K03209  wingless-type MMTV integration site family, member 1
Organism
vpc  Vicugna pacos (alpaca)
Pathway
vpc04150  mTOR signaling pathway
vpc04310  Wnt signaling pathway
vpc04390  Hippo signaling pathway
vpc04550  Signaling pathways regulating pluripotency of stem cells
vpc04916  Melanogenesis
vpc04934  Cushing syndrome
vpc05010  Alzheimer disease
vpc05022  Pathways of neurodegeneration - multiple diseases
vpc05165  Human papillomavirus infection
vpc05200  Pathways in cancer
vpc05205  Proteoglycans in cancer
vpc05207  Chemical carcinogenesis - receptor activation
vpc05217  Basal cell carcinoma
vpc05224  Breast cancer
vpc05225  Hepatocellular carcinoma
vpc05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:vpc00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102535386 (WNT1)
   04390 Hippo signaling pathway
    102535386 (WNT1)
   04150 mTOR signaling pathway
    102535386 (WNT1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102535386 (WNT1)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102535386 (WNT1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102535386 (WNT1)
   05205 Proteoglycans in cancer
    102535386 (WNT1)
   05207 Chemical carcinogenesis - receptor activation
    102535386 (WNT1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102535386 (WNT1)
   05226 Gastric cancer
    102535386 (WNT1)
   05217 Basal cell carcinoma
    102535386 (WNT1)
   05224 Breast cancer
    102535386 (WNT1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102535386 (WNT1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102535386 (WNT1)
   05022 Pathways of neurodegeneration - multiple diseases
    102535386 (WNT1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102535386 (WNT1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:vpc00536]
    102535386 (WNT1)
Glycosaminoglycan binding proteins [BR:vpc00536]
 Heparan sulfate / Heparin
  Morphogens
   102535386 (WNT1)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 102535386
NCBI-ProteinID: XP_031538912
UniProt: A0A6J3B0E2
LinkDB
Position
12
AA seq 340 aa
MRLTRGIVNVASSTNLLTDSKSLQLVLEPSLQLLSRKQRRLIRQNPGILHSVSGGLQSAV
RECKWQFRNRRWNCPTASGPHLFGKIVNRGCRETAFIFAITSAGVTHSVARSCSEGSIES
CTCDYRRRGPGGPDWHWGGCSDNIDFGRLFGREFVDSGEKGRDLRFLMNLHNNEAGRTTV
FSEMRQECKCHGMSGSCTVRTCWMRLPTLRAVGDVLRDRFDGASRVLYGNRGSNRASRAE
LLRLEPEDPAHKPPSPHDLVYFEKSPNFCTYSGRLGTAGTAGRACNSSSPALDGCELLCC
GRGHRTRTQRVTERCNCTFHWCCHVSCRNCTHTRVLHECL
NT seq 1023 nt   +upstreamnt  +downstreamnt
atgcgtctcaccaggggcatcgtgaacgtagcctcctccacgaacctgctgaccgattcc
aagagcctgcaactggtactcgagcccagcctgcagctgctcagccgcaaacagcggcgg
ctgatccgccagaaccctgggatcctgcacagtgtgagcggggggctgcagagcgctgtg
cgagagtgcaagtggcagttccggaaccgccgctggaactgtcccacggcttcagggccc
cacctcttcggcaaaatcgtcaaccgaggctgtcgggaaactgcatttatcttcgccatc
acctcagccggggtcacccattcggtggcgcgctcctgctcggagggctccatcgagtcc
tgcacgtgcgactaccggcggcgcggcccggggggtcccgattggcactgggggggctgc
agtgacaacattgacttcggccgcctctttggcagggagtttgtggactccggggagaag
gggcgggacctgcgcttcctcatgaaccttcacaacaacgaggcgggccgcacgacggtg
ttctctgagatgcgccaggagtgtaagtgccacggcatgtccggctcgtgcacggtgcgc
acgtgctggatgcggctgcccacactgcgcgccgtgggggacgtgctgcgcgaccgcttc
gatggcgcctcgcgcgtcctctacggcaaccgcggcagcaaccgcgcctcgcgggctgaa
ctgctgcgcctcgagccggaagacccagcgcacaagccgccctcccctcacgacctcgtc
tactttgagaaatcgcccaacttctgcacatacagcggacgcctgggtacagcgggcacg
gcggggcgcgcctgcaacagctcgtcgcccgcgctggacggctgcgagctgctctgctgt
ggccggggccaccgcacgcgcacgcagcgcgtcacggagcgctgcaactgcaccttccac
tggtgctgccacgtcagctgccgcaactgcacgcacacgcgtgtcctgcacgagtgcctg
tga

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