KEGG   Peromyscus maniculatus bairdii (prairie deer mouse): 102908613
Entry
102908613         CDS       T11302                                 
Symbol
Wnt10a
Name
(RefSeq) protein Wnt-10a
  KO
K01357  wingless-type MMTV integration site family, member 10
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
    102908613 (Wnt10a)
   04390 Hippo signaling pathway
    102908613 (Wnt10a)
   04150 mTOR signaling pathway
    102908613 (Wnt10a)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102908613 (Wnt10a)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102908613 (Wnt10a)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102908613 (Wnt10a)
   05205 Proteoglycans in cancer
    102908613 (Wnt10a)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102908613 (Wnt10a)
   05226 Gastric cancer
    102908613 (Wnt10a)
   05217 Basal cell carcinoma
    102908613 (Wnt10a)
   05224 Breast cancer
    102908613 (Wnt10a)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102908613 (Wnt10a)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102908613 (Wnt10a)
   05022 Pathways of neurodegeneration - multiple diseases
    102908613 (Wnt10a)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102908613 (Wnt10a)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pmav00536]
    102908613 (Wnt10a)
Glycosaminoglycan binding proteins [BR:pmav00536]
 Heparan sulfate / Heparin
  Morphogens
   102908613 (Wnt10a)
SSDB
Motif
Pfam: wnt DUF6973 DUF7539
Other DBs
NCBI-GeneID: 102908613
NCBI-ProteinID: XP_006972241
Ensembl: ENSPEMG00000007994
UniProt: A0A6I9L2R2
LinkDB
Position
13:complement(39835207..39847175)
AA seq 417 aa
MGSAHPHPWLRLPPRPQPRPELWALLFFLLLLAAAVPRSAPNDILGLRLPPEPVLNANTV
CLTLPGLSRRQMEVCVRHPDVAASAIQGIQIAIHECQHQFRDQRWNCSSLETRNKVPYES
PIFSRGFRESAFAYAIAAAGVVHAVSNACALGKLQACGCDASRRGDEEAFRRKLHRLQLD
ALQRGKGLSHGVPEHPALPPASPGLQDSWEWGGCSPDVGFGERFSKDFLDSREPHRDIHA
RMRLHNNRVGRQAVMENMRRKCKCHGTSGSCQLKTCWQVTPEFRAVGALLRNRFHRATLI
RPHNRNGGQLEPGPAGAPSPAPGTPGLRRRASHSDLVYFEKSPDFCEREPRLDSAGTVGR
LCNKSSSGPDGCGSMCCGRGHNILRQTRSERCHCRFHWCCFVVCEECRITEWVSVCK
NT seq 1254 nt   +upstreamnt  +downstreamnt
atgggcagcgcccaccctcacccctggctgcggctcccaccccggccccagccgcggcct
gagctctgggcgctcctgttcttcctactgctgctggctgccgctgtgcccaggtcagca
cccaacgacatcctgggcctccgcctacccccagagcctgtactcaacgccaacacagtg
tgcctgacattgcccggcctgagccggcggcagatggaggtgtgcgtgcgtcaccctgac
gtggccgcctctgctatccagggcatccagatcgccatccacgagtgccagcatcagttc
cgggaccagcgctggaactgttccagcctggagactcggaacaaagtcccctacgagagt
cctatcttcagtagaggttttcgagagagtgctttcgcctacgccatcgcagctgccggg
gtggtgcacgcagtgtccaacgcatgcgccttgggtaaactacaggcttgcggttgcgac
gcctccaggcgtggggacgaagaagccttccgtcggaagctgcaccgcctgcagctggac
gcgctgcagcgcggtaagggcctgagccacggggtcccagaacaccctgctctgccccct
gccagcccaggcctgcaggactcctgggagtggggtggctgcagcccggatgtgggcttc
ggagaacgcttctccaaggactttctggactcccgggagcctcacagagacattcacgcg
cgcatgagactccacaacaaccgtgtcggcaggcaggcggtgatggagaacatgcggcga
aagtgcaagtgccatggcacctcaggcagctgtcagctcaagacgtgctggcaggtgacg
cccgagtttcgtgccgtgggggcgctgctgcgcaaccgcttccaccgcgccacgctcatc
cggccgcacaaccgcaacggtggccagctggagcccggccccgcgggggcaccctcgcca
gctcccggcactccagggctgcgccgaagggccagccactccgacctggtctacttcgag
aaatcgcccgacttctgtgagcgcgagcctcgcctggactcggcgggcaccgtgggccgc
ctgtgcaacaagagcagctcgggcccggacggctgcggcagcatgtgctgtggccgcggc
cacaacatcctgcgccagacgcgcagtgagcgctgccactgccgtttccactggtgctgc
ttcgtggtctgcgaagaatgccgaatcaccgagtgggtcagcgtctgcaagtga

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