KEGG   Mustela putorius furo (domestic ferret): 106004732
Entry
106004732         CDS       T07239                                 
Name
(RefSeq) atherin-like
  KO
K00444  wingless-type MMTV integration site family, member 5
Organism
mpuf  Mustela putorius furo (domestic ferret)
Pathway
mpuf04150  mTOR signaling pathway
mpuf04310  Wnt signaling pathway
mpuf04360  Axon guidance
mpuf04390  Hippo signaling pathway
mpuf04519  Cadherin signaling
mpuf04550  Signaling pathways regulating pluripotency of stem cells
mpuf04916  Melanogenesis
mpuf04934  Cushing syndrome
mpuf05010  Alzheimer disease
mpuf05022  Pathways of neurodegeneration - multiple diseases
mpuf05165  Human papillomavirus infection
mpuf05200  Pathways in cancer
mpuf05205  Proteoglycans in cancer
mpuf05217  Basal cell carcinoma
mpuf05224  Breast cancer
mpuf05225  Hepatocellular carcinoma
mpuf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mpuf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    106004732
   04390 Hippo signaling pathway
    106004732
   04150 mTOR signaling pathway
    106004732
  09133 Signaling molecules and interaction
   04519 Cadherin signaling
    106004732
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    106004732
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    106004732
  09158 Development and regeneration
   04360 Axon guidance
    106004732
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    106004732
   05205 Proteoglycans in cancer
    106004732
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    106004732
   05226 Gastric cancer
    106004732
   05217 Basal cell carcinoma
    106004732
   05224 Breast cancer
    106004732
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    106004732
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    106004732
   05022 Pathways of neurodegeneration - multiple diseases
    106004732
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    106004732
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mpuf00536]
    106004732
Glycosaminoglycan binding proteins [BR:mpuf00536]
 Heparan sulfate / Heparin
  Morphogens
   106004732
SSDB
Motif
Pfam: wnt DUF6973 K_channel_TID
Other DBs
NCBI-GeneID: 106004732
NCBI-ProteinID: XP_012906463
LinkDB
Position
Unknown
AA seq 304 aa
LLSRAFWEVSFPRFSGAGGNTSPALPERCGRFSVKSKGVCVGVWGVCCSCHLPLPPSVGR
LSCLLPWGWGPAPGVWVLGLGRPRPLCPGPLGGWGGWGSPGALGARGRRQAPGDPRVPPA
GSRETAFTYAVSAAGVVNAMSRACREGELSTCGCSRAARPKDLPRDWLWGGCGDNIDYGY
RFAKEFVDARERERIHAKGSYESARILMNLHNNEAGRRVSPPPAPPARSAPSSPAPAPAA
RSGPAGVPRLGPPVLRPSVPPCAALQVYLPLGRSPGRPAPSFPLGLCPSLLPCPPPSLPP
SPPT
NT seq 912 nt   +upstreamnt  +downstreamnt
cttctttcacgtgcgttttgggaagtaagttttccaagattttcaggggctggagggaac
accagtccagcgctgcctgagcgctgtggccgcttcagtgtcaagagtaaaggtgtgtgt
gtgggtgtgtggggggtctgctgctcctgtcacttgccgctgccgccgagtgttgggcgg
ttgtcctgcctcctcccctgggggtgggggccggccccgggggtgtgggtattagggctg
gggcgcccccggcccctctgccccgggccgctgggtgggtggggtgggtggggctcccca
ggggccctcggagcccggggccgccggcaggcgccgggtgacccccgcgtcccgcccgca
ggcagccgcgagacggccttcacgtacgcggtgagcgccgcgggggtggtgaacgccatg
agccgcgcgtgccgcgagggcgagctgtccacctgcggctgcagccgcgccgcgcgcccc
aaggacctgccgcgggactggctgtggggcggctgcggggacaacatcgactacggctac
cgcttcgccaaggagttcgtggatgcgcgcgagcgggagcgcatccacgccaagggctcg
tacgagagcgcgcgcatcctcatgaacttgcacaacaacgaggccggccgcagggtgagt
cctccgcccgccccgcctgcccgctccgccccatcatcccccgcccccgcccccgccgcc
cgctccggtcccgctggggtccccaggctcggcccgccggtcctccggccctcggtgccg
ccctgcgccgccctccaggtgtacctgcccctcggtcgctctcccgggcgtccggcccct
tctttccctttaggactctgcccttcgctgctcccctgtccgcctccttcccttcctccc
tccccacctaca

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