KEGG   Neogale vison (American mink): 122891308
Entry
122891308         CDS       T08764                                 
Symbol
WNT1
Name
(RefSeq) proto-oncogene Wnt-1
  KO
K03209  wingless-type MMTV integration site family, member 1
Organism
nvs  Neogale vison (American mink)
Pathway
nvs04150  mTOR signaling pathway
nvs04310  Wnt signaling pathway
nvs04390  Hippo signaling pathway
nvs04550  Signaling pathways regulating pluripotency of stem cells
nvs04916  Melanogenesis
nvs04934  Cushing syndrome
nvs05010  Alzheimer disease
nvs05022  Pathways of neurodegeneration - multiple diseases
nvs05165  Human papillomavirus infection
nvs05200  Pathways in cancer
nvs05205  Proteoglycans in cancer
nvs05207  Chemical carcinogenesis - receptor activation
nvs05217  Basal cell carcinoma
nvs05224  Breast cancer
nvs05225  Hepatocellular carcinoma
nvs05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:nvs00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    122891308 (WNT1)
   04390 Hippo signaling pathway
    122891308 (WNT1)
   04150 mTOR signaling pathway
    122891308 (WNT1)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    122891308 (WNT1)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    122891308 (WNT1)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    122891308 (WNT1)
   05205 Proteoglycans in cancer
    122891308 (WNT1)
   05207 Chemical carcinogenesis - receptor activation
    122891308 (WNT1)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    122891308 (WNT1)
   05226 Gastric cancer
    122891308 (WNT1)
   05217 Basal cell carcinoma
    122891308 (WNT1)
   05224 Breast cancer
    122891308 (WNT1)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    122891308 (WNT1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    122891308 (WNT1)
   05022 Pathways of neurodegeneration - multiple diseases
    122891308 (WNT1)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    122891308 (WNT1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:nvs00536]
    122891308 (WNT1)
Glycosaminoglycan binding proteins [BR:nvs00536]
 Heparan sulfate / Heparin
  Morphogens
   122891308 (WNT1)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 122891308
NCBI-ProteinID: XP_044082802
UniProt: A0A8C7ATA3
LinkDB
Position
12:85343274..85346376
AA seq 370 aa
MGHWAQLPGWVSATLLLALAALPAALAANSSGRWWGIVNVASSTNLLTDSKSLQLVLEPS
LQLLSRKQRRLIRQNPGILHSVSGGLQSAVRECKWQFRNRRWNCPTAPGPHLFGKIVNRG
CRETAFIFAITSAGVTHSVARSCSEGSIESCTCDYRRRGPGGPDWHWGGCSDNIDFGRLF
GREFVDSGEKGRDLRFLMNLHNNEAGRTTVFSEMRQECKCHGMSGSCTVRTCWMRLPTLR
AVGDVLRDRFDGASRVLYGNRGSNRASRAELLRLEPEDPAHKPPSPHDLVYFEKSPNFCT
YSGRLGTAGTAGRACNSSSPALDGCELLCCGRGHRTRTQRVTERCNCTFHWCCHVSCRNC
THTRVLHECL
NT seq 1113 nt   +upstreamnt  +downstreamnt
atggggcactgggcgcagctgcccggctgggtttctgctacgctgttgctggcgctggcc
gctctgcctgcagccctggccgccaacagcagtggccgatggtggggcatcgtgaacgta
gcctcctccacgaacctgctgaccgactccaagagtctacaactggtgctggagcccagt
cttcagctgctgagccgcaaacagcggcggctgatacgccagaacccggggatcctgcac
agcgtgagcgggggactgcagagcgcggtgcgagagtgcaagtggcagttccgcaaccgc
cgctggaactgccccacggctccggggccccacctcttcggcaagatcgtcaatcgaggc
tgtcgggaaacggcgtttatcttcgccatcacctccgcaggggttacgcattcagtggca
cgctcctgctcggagggctccatcgagtcttgcacgtgcgactaccggcggcggggtccc
gggggccccgattggcactgggggggctgcagcgacaacatcgacttcggccgcctcttc
ggcagggagtttgtggactccggggagaaggggcgggacctgcgcttcctcatgaacctt
cacaacaacgaggcgggccgcacgaccgtgttctccgagatgcgccaggagtgcaagtgc
cacgggatgtcgggctcgtgcacggtgcgcacgtgctggatgcggctgcccacgctgcgt
gcagtgggcgacgtgctacgcgacagattcgatggcgcctcgcgcgtactgtacggcaac
cgcggcagcaaccgcgcctcgcgggcagagctgctgcgcttggagcccgaagaccccgcg
cacaagccgccctccccccacgacctcgtctactttgagaaatcgcccaatttctgcacg
tacagcggacgcctggggacagcgggcacggcggggcgcgcctgcaacagctcgtcgccc
gcgctggacggctgcgagctgctctgttgtggccggggccaccgcacgcgcacacagcgc
gtcacggagcgctgcaactgcacctttcactggtgctgccacgtcagttgccgcaactgc
acgcacacgcgtgtactgcatgagtgtctgtga

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