KEGG   Loxodonta africana (African savanna elephant): 100662057
Entry
100662057         CDS       T04351                                 
Symbol
WNT9A
Name
(RefSeq) protein Wnt-9a
  KO
K01064  wingless-type MMTV integration site family, member 9
Organism
lav  Loxodonta africana (African savanna elephant)
Pathway
lav04150  mTOR signaling pathway
lav04310  Wnt signaling pathway
lav04390  Hippo signaling pathway
lav04550  Signaling pathways regulating pluripotency of stem cells
lav04916  Melanogenesis
lav04934  Cushing syndrome
lav05010  Alzheimer disease
lav05022  Pathways of neurodegeneration - multiple diseases
lav05165  Human papillomavirus infection
lav05200  Pathways in cancer
lav05205  Proteoglycans in cancer
lav05217  Basal cell carcinoma
lav05224  Breast cancer
lav05225  Hepatocellular carcinoma
lav05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:lav00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100662057 (WNT9A)
   04390 Hippo signaling pathway
    100662057 (WNT9A)
   04150 mTOR signaling pathway
    100662057 (WNT9A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100662057 (WNT9A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100662057 (WNT9A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100662057 (WNT9A)
   05205 Proteoglycans in cancer
    100662057 (WNT9A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100662057 (WNT9A)
   05226 Gastric cancer
    100662057 (WNT9A)
   05217 Basal cell carcinoma
    100662057 (WNT9A)
   05224 Breast cancer
    100662057 (WNT9A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100662057 (WNT9A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100662057 (WNT9A)
   05022 Pathways of neurodegeneration - multiple diseases
    100662057 (WNT9A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100662057 (WNT9A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:lav00536]
    100662057 (WNT9A)
Glycosaminoglycan binding proteins [BR:lav00536]
 Heparan sulfate / Heparin
  Morphogens
   100662057 (WNT9A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100662057
NCBI-ProteinID: XP_003421261
LinkDB
Position
Unknown
AA seq 639 aa
MASETPAFHPRFSATDAGEQLVAEVAVWVAGASRQEGRLSGRMLGSTHPPVLLMVEGSDA
ISATACQWRESVHVHLGSALLLCEAGGPKCQHHHMPQAVGPLGWLHAEPTCWTVVKGSLR
QEITFLGGGEVEQGASGGEEGSSGPHIASELRGAVWMEGMTLLGGWSLSCPGPQQLTWLQ
GSRQASLRLLRGQLDVALGPPLAVGSWMWLWAPLTQWAARDGSGQCCSPCPQLWGMEPAC
LCKLTRRSHRCPHSLNLLWIQTCWKGLASPPASEMLAPHPAARLARLGTVQSPESAGNSC
FCVPRLTGSEPLTILPLTLEPEAAAAKAHYKACDRLKLERKQRRMCRRDPGVAETLVEAI
SMSALECQYQFRFERWNCTLEGRYRASLLKRGFKETAFLYAISSAGLTHALAKACSAGRM
ERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVKEFLGRRSSKDLRARVDFHNNLVGVKV
IKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVGKHLKHKYETALKVGSTTNEATGEAGD
ISPPRGRAPGAGGSDPLPRTPELVHLDDSPSFCLAGRFSPGTAGRKCHREKNCESICCGR
GHNTQSRAVTRPCQCQVRWCCYVECKQCTQREEVYTCKG
NT seq 1920 nt   +upstreamnt  +downstreamnt
atggcttctgagacgccagccttccaccctaggttctcggctaccgacgccggggagcag
ctggtggcagaggtggctgtttgggtggctggggccagtcggcaggagggaagactgtcg
gggcggatgctggggtctacccaccccccagtgctactcatggtggaaggctcagatgcc
atcagtgccaccgcctgccagtggagggagtctgtgcatgtgcacctgggctctgccctg
ctcctgtgtgaagccggggggcccaagtgccagcaccaccacatgccacaggctgtaggt
cccctaggctggctgcatgctgagcctacctgctggacagttgtgaagggcagcctcagg
caggagatcacctttctgggagggggagaggtggagcagggtgcctcaggaggggaggag
ggtagcagtggaccccacatagcttcagagctcagaggggctgtgtggatggagggcatg
accctcctgggtggctggagcctgtcctgtccaggcccccagcagctcacttggctgcag
ggcagcaggcaggccagcctgcggctgcttcgtgggcagctggatgtggctctgggcccc
cctctcgcagtgggcagctggatgtggctctgggcccccctcacccagtgggcagcccgg
gatggctctggacagtgctgttctccttgcccacagctgtggggcatggagcctgcctgc
ctctgtaagctgacccgcaggagtcacagatgtccacacagcctgaacctgctgtggata
cagacctgctggaagggccttgcctctcccccagcctccgagatgctggcccctcaccca
gctgctcggctcgcccgcctggggacagtgcagtctcctgagagtgctggtaactcttgc
ttctgtgtgcccaggctgacgggcagtgagcccctgaccatcctccctctgaccctggag
cctgaggccgcggccgccaaggcacactacaaggcctgtgaccggctgaagctggagcgg
aagcagcggcgcatgtgccgccgggacccaggggtggccgagacgctggtggaggccatc
agcatgagcgcccttgagtgccagtaccagttccgtttcgaaagatggaactgcaccctg
gagggccgctaccgggcgagcctgctcaagcgaggcttcaaggagacagccttcctgtac
gccatctcctcggccgggctgacccacgcgctggccaaggcctgcagcgccggccgcatg
gagcgctgcacctgtgacgaggcgcctgacctggagaaccgtgaggcctggcagtggggc
ggctgtggggacaacctcaagtacagcagcaagttcgtcaaggaattcctgggccgcagg
tcgagcaaggacctgcgggcccgcgtggacttccacaacaacctcgtaggcgtgaaggtg
atcaaggccggggtggagaccacgtgcaagtgccatggtgtgtctggctcctgcacagtt
cggacctgctggcgccagctggcacccttccacgaggtgggcaagcacctgaagcacaag
tatgagactgcgctcaaggtgggcagcaccaccaacgaggccacaggcgaggcaggtgac
atctcgccacctcgaggtcgagcaccgggggcgggtggcagcgacccactgcctcgcacc
cccgagctggtgcatctggacgactcgcccagcttctgtctggctggccgcttctccccg
ggcaccgccggccgtaagtgccaccgtgagaagaactgtgagagcatctgctgcgggcgt
ggccacaacacgcagagccgggccgtcacacggccctgccagtgccaggtgcgctggtgc
tgctacgtggagtgcaagcagtgcacgcagcgcgaggaggtctacacctgcaagggctga

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