KEGG   Trachypithecus francoisi (Francois's langur): 117074665
Entry
117074665         CDS       T07225                                 
Symbol
WNT9A
Name
(RefSeq) protein Wnt-9a
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
tfn  Trachypithecus francoisi (Francois's langur)
Pathway
tfn04150  mTOR signaling pathway
tfn04310  Wnt signaling pathway
tfn04390  Hippo signaling pathway
tfn04550  Signaling pathways regulating pluripotency of stem cells
tfn04916  Melanogenesis
tfn04934  Cushing syndrome
tfn05010  Alzheimer disease
tfn05022  Pathways of neurodegeneration - multiple diseases
tfn05165  Human papillomavirus infection
tfn05200  Pathways in cancer
tfn05205  Proteoglycans in cancer
tfn05217  Basal cell carcinoma
tfn05224  Breast cancer
tfn05225  Hepatocellular carcinoma
tfn05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:tfn00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    117074665 (WNT9A)
   04390 Hippo signaling pathway
    117074665 (WNT9A)
   04150 mTOR signaling pathway
    117074665 (WNT9A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    117074665 (WNT9A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    117074665 (WNT9A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    117074665 (WNT9A)
   05205 Proteoglycans in cancer
    117074665 (WNT9A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    117074665 (WNT9A)
   05226 Gastric cancer
    117074665 (WNT9A)
   05217 Basal cell carcinoma
    117074665 (WNT9A)
   05224 Breast cancer
    117074665 (WNT9A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    117074665 (WNT9A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117074665 (WNT9A)
   05022 Pathways of neurodegeneration - multiple diseases
    117074665 (WNT9A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    117074665 (WNT9A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:tfn00536]
    117074665 (WNT9A)
Glycosaminoglycan binding proteins [BR:tfn00536]
 Heparan sulfate / Heparin
  Morphogens
   117074665 (WNT9A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 117074665
NCBI-ProteinID: XP_033052221
LinkDB
Position
Unknown
AA seq 365 aa
MLDGSPLARWLATAFGLTLLLAALRPSAAYFGLTGSEPLTVLPLTLEPEAAAQAHYKACD
RLKLERKQRRMCRRDPGVAETLVEAVSMSALECQFQFRFERWNCTLEGRYRASLLKRGFK
ETAFLYAISSAGLTHALAKACSAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVK
EFLGRRSSKDLRARVDFHNNLVGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVG
KHLKHKYETALKVGSTTNEAAGEAGAISPPRGRASGTGGSDPLPRTPELVHLDDSPSFCL
AGRFSPGTAGRRCHREKNCESICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEV
YTCKG
NT seq 1098 nt   +upstreamnt  +downstreamnt
atgctggatgggtccccgctggcgcgctggctggccacggccttcgggctgacgctgctg
ctcgccgcgctgcgcccttctgccgcctacttcgggctgacgggcagcgagcccctgact
gtcctcccgctgaccctggagcccgaggcggccgcccaggcacactacaaggcctgcgac
cggctgaagctggagcggaagcagcggcgcatgtgccgccgggacccgggtgtggcagag
acgctggtggaggccgtgagcatgagtgcgcttgagtgccagttccaattccgctttgag
cgctggaactgcacgctggagggccgctaccgggccagcctactcaagcgaggcttcaag
gagactgccttcctctatgccatctcctcggctggcctgacgcacgcactggccaaggca
tgcagcgcaggccgcatggagcgctgtacctgcgatgaggcgcccgacctggagaaccgt
gaggcctggcagtgggggggctgcggagacaacctcaagtacagtagcaagttcgtcaag
gagttcctgggcagacggtcaagcaaggatctgcgagcccgtgtggacttccacaacaac
ctcgtgggtgtgaaggtgatcaaggctggagtggagaccacctgcaagtgccacggcgtg
tcaggctcatgcacagtgcggacctgctggcggcagctggcgcccttccatgaggtgggc
aagcacctgaagcacaagtacgagacagcactcaaggtgggcagcaccaccaacgaagct
gcaggcgaggcaggcgccatttccccaccacggggccgtgcctcagggacgggcggcagt
gacccgctaccccgcactccagagctggtgcacctggacgactcgcctagcttctgcctg
gccggccgcttctccccgggcaccgctggccgtaggtgccaccgcgagaagaactgcgag
agcatctgctgcggccgcggccataacacacagagccgggtggtgacgaggccctgccag
tgccaggtgcgttggtgctgctatgtggagtgcaggcagtgcacacagcgtgaggaggtc
tacacctgcaagggctga

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