KEGG   Propithecus coquereli (Coquerel's sifaka): 105808138
Entry
105808138         CDS       T08746                                 
Symbol
WNT9A
Name
(RefSeq) protein Wnt-9a isoform X1
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
pcoq  Propithecus coquereli (Coquerel's sifaka)
Pathway
pcoq04150  mTOR signaling pathway
pcoq04310  Wnt signaling pathway
pcoq04390  Hippo signaling pathway
pcoq04550  Signaling pathways regulating pluripotency of stem cells
pcoq04916  Melanogenesis
pcoq04934  Cushing syndrome
pcoq05010  Alzheimer disease
pcoq05022  Pathways of neurodegeneration - multiple diseases
pcoq05165  Human papillomavirus infection
pcoq05200  Pathways in cancer
pcoq05205  Proteoglycans in cancer
pcoq05217  Basal cell carcinoma
pcoq05224  Breast cancer
pcoq05225  Hepatocellular carcinoma
pcoq05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pcoq00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105808138 (WNT9A)
   04390 Hippo signaling pathway
    105808138 (WNT9A)
   04150 mTOR signaling pathway
    105808138 (WNT9A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105808138 (WNT9A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105808138 (WNT9A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105808138 (WNT9A)
   05205 Proteoglycans in cancer
    105808138 (WNT9A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105808138 (WNT9A)
   05226 Gastric cancer
    105808138 (WNT9A)
   05217 Basal cell carcinoma
    105808138 (WNT9A)
   05224 Breast cancer
    105808138 (WNT9A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105808138 (WNT9A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105808138 (WNT9A)
   05022 Pathways of neurodegeneration - multiple diseases
    105808138 (WNT9A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105808138 (WNT9A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pcoq00536]
    105808138 (WNT9A)
Glycosaminoglycan binding proteins [BR:pcoq00536]
 Heparan sulfate / Heparin
  Morphogens
   105808138 (WNT9A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 105808138
NCBI-ProteinID: XP_012497156
Ensembl: ENSPCOG00000015468
UniProt: A0A2K6F322
LinkDB
Position
Unknown
AA seq 365 aa
MLDGPLLARWLAAAFGLTLLLAALRPSAAYFGLTGSEPLTILPLTLEPEAAAQAHYKACD
RLKLERKQRRMCRRDPGVAETLVEAVSMSALECQFQFRFERWNCTLEGRYRASLLKRGFK
ETAFLYAISSAGLTHALAKACSAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVK
EFLGRRSSKDLRARVDFHNNLVGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVG
KHLKHKYETALKVGSTTNEATGEAGAISPPRGRASGAGGSDPLPRTPELVHLDDSPSFCL
AGRFSPGTAGRRCHREKNCESICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEV
YTCKG
NT seq 1098 nt   +upstreamnt  +downstreamnt
atgctggatgggcccctgctggcgcgctggctggccgcggccttcgggctgacgctgctg
ctcgccgcgctgcgcccttcggccgcctacttcgggctgacgggcagcgagcctctgacc
atcctcccgctcacactggagcccgaggcagcagcccaggcgcactacaaggcctgcgac
cggctgaagctggagcggaagcagcggcgcatgtgccgccgggatccgggcgtggccgag
acgctggtggaggcggtcagcatgagcgcgctggagtgccagttccagttccgcttcgag
cgctggaactgcaccttggagggccgctaccgggccagcctgctcaagcgaggcttcaag
gagaccgccttcctctacgccatctcctccgccggcctgacgcacgcgctggccaaggcg
tgcagcgcggggcgcatggagcgctgcacgtgcgacgaggcgccggacctggagaaccgc
gaggcctggcagtggggaggctgcggggacaacctcaagtacagcagcaagttcgtcaag
gagttcctgggcaggcggtcgagcaaggacctgcgggcccgcgtggacttccacaacaac
ctcgtgggcgtgaaggtgatcaaggccggcgtcgagaccacctgcaagtgccacggcgtg
tcgggctcgtgcacggtgcggacctgctggcggcagctggcgcccttccacgaggtgggc
aaacacctgaagcacaagtacgagacggcgctcaaagtgggcagcaccaccaacgaggcc
accggtgaggcgggcgccatctccccgccgcggggacgggcctcgggggcgggcggcagc
gacccgctgccccgcaccccggagctggtgcacctggacgactcgcccagcttctgcttg
gccggccgcttctccccgggcacggccggccgcaggtgccaccgcgagaagaactgcgag
agcatctgctgcggccgcggccacaacacgcagagccgggtggtcacgaggccctgccag
tgccaggtgcgctggtgctgctacgtggagtgcaggcagtgcacgcagcgcgaggaggtc
tacacctgcaagggctga

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