KEGG   Loxodonta africana (African savanna elephant): 100668409
Entry
100668409         CDS       T04351                                 
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a
  KO
K00714  wingless-type MMTV integration site family, member 8
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
    100668409 (WNT8A)
   04390 Hippo signaling pathway
    100668409 (WNT8A)
   04150 mTOR signaling pathway
    100668409 (WNT8A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100668409 (WNT8A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100668409 (WNT8A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100668409 (WNT8A)
   05205 Proteoglycans in cancer
    100668409 (WNT8A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100668409 (WNT8A)
   05226 Gastric cancer
    100668409 (WNT8A)
   05217 Basal cell carcinoma
    100668409 (WNT8A)
   05224 Breast cancer
    100668409 (WNT8A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100668409 (WNT8A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100668409 (WNT8A)
   05022 Pathways of neurodegeneration - multiple diseases
    100668409 (WNT8A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100668409 (WNT8A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:lav00536]
    100668409 (WNT8A)
Glycosaminoglycan binding proteins [BR:lav00536]
 Heparan sulfate / Heparin
  Morphogens
   100668409 (WNT8A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100668409
NCBI-ProteinID: XP_023405096
LinkDB
Position
Unknown
AA seq 352 aa
MGDLIMLWVAVGICWTTLSASAWSVNNFLITGPKAYLTYTTSVALGAQSGVEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYTITKNCSMGDFENCGCDESKNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC
KCHGISGSCSIQTCWLQLADFREMGDYLKAKYDRALKIEMDKPRLRAGNSAEGRWAPTAA
FLPSAEAELIFLEESPDYCIRNSSLGIYGTEGRECLQNSHNTSRWEQRSCGRLCTECGLQ
VEERRTEAISSCNCKFQWCCTVKCDQCRHVVNKYYCMRSPDSARSQDKGSAR
NT seq 1059 nt   +upstreamnt  +downstreamnt
atgggggacctgattatgctctgggtggctgtgggcatatgctggaccaccctcagtgct
tctgcctggtcagtgaacaacttcctgataacaggtcccaaggcctatctgacctacacc
accagtgtggccctgggggcccagagtggcgttgaggagtgtaagttccaatttgcttgg
gaacgctggaactgtcctgaaaatgctctgcagctctctactcacaacaggctgagaagt
gccactagggagacttccttcattcacgcaatcagctctgcgggggtcatgtacaccatt
accaagaattgtagcatgggagactttgaaaactgtggctgtgatgagtcaaaaaatgga
aaaacaggaggccacggctggatctggggaggctgcagcgacaatgtggaatttggagaa
agaatctccaagctctttgtggacagcctggagaaggggaaggatgccagagccctgatg
aatcttcataacaatagggcaggaaggctggcagtgagagccaccatgaagaggacctgc
aaatgtcatggcatctcgggaagctgcagcatccagacatgctggctgcagctagctgac
ttccgggagatgggagactacctaaaggccaagtatgaccgggcactgaaaattgagatg
gataagccgcggctaagggctgggaacagtgctgagggccgctgggcacccaccgcggcc
ttccttcctagtgcagaggctgagctgatcttcttggaggagtcaccagattactgtatc
cgcaattccagcctgggcatctatggcacagagggtcgagagtgtctgcagaacagccac
aacacatccaggtgggagcaacgcagctgtgggcgcctgtgcaccgagtgtggtctgcag
gtcgaagagaggagaacagaggccatcagcagctgtaactgcaaattccagtggtgctgc
acagtgaagtgcgaccagtgtaggcacgtagtcaacaagtactattgcatgcgctccccg
gacagcgcccggtcccaagacaagggcagtgcccgatag

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