KEGG   Peromyscus maniculatus bairdii (prairie deer mouse): 102911140
Entry
102911140         CDS       T11302                                 
Symbol
Wnt6
Name
(RefSeq) protein Wnt-6
  KO
K00445  wingless-type MMTV integration site family, member 6
Organism
pmav  Peromyscus maniculatus bairdii (prairie deer mouse)
Pathway
pmav04150  mTOR signaling pathway
pmav04310  Wnt signaling pathway
pmav04390  Hippo signaling pathway
pmav04550  Signaling pathways regulating pluripotency of stem cells
pmav04916  Melanogenesis
pmav04934  Cushing syndrome
pmav05010  Alzheimer disease
pmav05022  Pathways of neurodegeneration - multiple diseases
pmav05165  Human papillomavirus infection
pmav05200  Pathways in cancer
pmav05205  Proteoglycans in cancer
pmav05217  Basal cell carcinoma
pmav05224  Breast cancer
pmav05225  Hepatocellular carcinoma
pmav05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pmav00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102911140 (Wnt6)
   04390 Hippo signaling pathway
    102911140 (Wnt6)
   04150 mTOR signaling pathway
    102911140 (Wnt6)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102911140 (Wnt6)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102911140 (Wnt6)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102911140 (Wnt6)
   05205 Proteoglycans in cancer
    102911140 (Wnt6)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102911140 (Wnt6)
   05226 Gastric cancer
    102911140 (Wnt6)
   05217 Basal cell carcinoma
    102911140 (Wnt6)
   05224 Breast cancer
    102911140 (Wnt6)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102911140 (Wnt6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102911140 (Wnt6)
   05022 Pathways of neurodegeneration - multiple diseases
    102911140 (Wnt6)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102911140 (Wnt6)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pmav00536]
    102911140 (Wnt6)
Glycosaminoglycan binding proteins [BR:pmav00536]
 Heparan sulfate / Heparin
  Morphogens
   102911140 (Wnt6)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 102911140
NCBI-ProteinID: XP_006972337
Ensembl: ENSPEMG00000013371
LinkDB
Position
13:complement(39854079..39867170)
AA seq 365 aa
MLPPVPSRLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQSEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRVLQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPSGLLGTPGPPGPTGSPDASAAWEWGGCGDDVDFGD
EKSRLFMDAQHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSSAPDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq 1098 nt   +upstreamnt  +downstreamnt
atgctgccacccgtgccctcccgcctcgggctgctgctgctgctgctcttgtgccccgcg
cacgtcgggggactgtggtgggctgtgggtagccccctggtcatggatcctaccagcatc
tgcaggaaggccaggcggctggcaggacggcaggctgagctgtgccagtcagagccggaa
gtggtggcagagctcgcccggggcgcaaggctgggggtccgagaatgtcagttccagttc
cgtttccgccgctggaactgctccagtcacagcaaggcctttgggcgcgtcttgcagcag
gacatccgagagacagccttcgtgtttgcgattactgcagccggcgccagccacgcggtc
acgcaggcctgttccatgggagaactcctgcagtgcggatgccaggcaccccgcgggcga
gcaccgcctaggccctctggccttctgggcactcctggacctccagggccaacaggttcc
ccagatgccagcgccgcctgggagtggggaggctgcggagacgatgtggacttcggggat
gagaagtcaaggctctttatggatgcccagcacaagcggggacgtggagacatccgggca
ctggtgcagctgcacaacaatgaggcgggcaggctggcggtgcggagccacacgcgcacc
gaatgtaagtgccacggcctttcgggttcgtgcgcgctgcgcacctgctggcagaagctg
cctccgttccgcgaggtgggcgcacggctgctggaacgcttccacggcgcctcgcgcgtc
atgggcaccaacgacggcaaagccctgctgcctgcagtccgcacgctcaagcctcccggc
cgagccgacctcctctacgccgccgactcgcccgacttctgcgcccccaaccggcgcacc
ggctcgcccggcacgcgcggccgcgcctgcaacagcagtgccccggacctcagcggctgc
gacctgttgtgctgcggtcgcggacaccgccaggagagcgtacagctcgaggagaactgc
ctgtgccgcttccactggtgctgcgtggtgcagtgccaccgctgccgcgtgcgcaaggag
ctcagcctgtgcctctga

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