KEGG   Loxodonta africana (African savanna elephant): 100662337
Entry
100662337         CDS       T04351                                 
Symbol
WNT3A
Name
(RefSeq) protein Wnt-3a
  KO
K00312  wingless-type MMTV integration site family, member 3
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
lav05206  MicroRNAs 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
    100662337 (WNT3A)
   04390 Hippo signaling pathway
    100662337 (WNT3A)
   04150 mTOR signaling pathway
    100662337 (WNT3A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100662337 (WNT3A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100662337 (WNT3A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100662337 (WNT3A)
   05206 MicroRNAs in cancer
    100662337 (WNT3A)
   05205 Proteoglycans in cancer
    100662337 (WNT3A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100662337 (WNT3A)
   05226 Gastric cancer
    100662337 (WNT3A)
   05217 Basal cell carcinoma
    100662337 (WNT3A)
   05224 Breast cancer
    100662337 (WNT3A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100662337 (WNT3A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100662337 (WNT3A)
   05022 Pathways of neurodegeneration - multiple diseases
    100662337 (WNT3A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100662337 (WNT3A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:lav00536]
    100662337 (WNT3A)
Glycosaminoglycan binding proteins [BR:lav00536]
 Heparan sulfate / Heparin
  Morphogens
   100662337 (WNT3A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 100662337
NCBI-ProteinID: XP_023396129
LinkDB
Position
Unknown
AA seq 236 aa
MATGGEGTWHGVQDERVYVIQGAKALRGGTCGDRGGKMRSLAIGHQYSSLGTQPILCASI
PGLVPKQLRFCRNYVEIMPSVAEGVKIGIQECQHQFRGRRWNCTTVNNSLAIFGPVLDKA
TRESAFVHAIASAGVAFAVTRSCAEGSAAICGCSGRHQGSPGEGWKWGGCSEDIEFGGMV
SREFADARENRPDARSAMNRHNNEAGRQVCPGEMHPEQGCAGYPGGCGLVWRKASG
NT seq 711 nt   +upstreamnt  +downstreamnt
atggccacagggggtgagggcacctggcatggtgttcaggatgagagggtgtacgtgatc
caaggagcaaaggcccttcggggcgggacttgtggagacagaggtgggaaaatgaggtcc
ctggccatcgggcaccagtactcctctctgggcactcagcccatcctctgtgccagcatc
cccggcctagtgcccaagcagctgcgcttctgccggaactacgtggagatcatgcccagt
gtggcagaaggcgtcaagatcggcatccaggagtgccagcaccagttccgtggccgccga
tggaactgcaccaccgtcaacaacagcctggccatctttgggcctgtgttggacaaagcc
accagggagtcggccttcgtccatgccattgcctcggccggcgtggccttcgctgtgacc
cgctcctgcgcagagggttctgctgccatctgcggctgcagtggccgccatcagggctca
ccaggcgaaggctggaagtggggcggctgcagtgaggacatcgagtttggtgggatggtg
tctcgggagttcgcagatgccagggagaaccgacctgatgcccgctcagccatgaaccgc
cacaacaacgaggctgggcgccaggtatgtcctggggaaatgcaccctgagcaggggtgt
gctgggtaccctggggggtgtggcctggtgtggcgcaaagcttctgggtaa

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