KEGG   Trachypithecus francoisi (Francois's langur): 117064599
Entry
117064599         CDS       T07225                                 
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a
  KO
K00714  wingless-type MMTV integration site family, member 8
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
    117064599 (WNT8A)
   04390 Hippo signaling pathway
    117064599 (WNT8A)
   04150 mTOR signaling pathway
    117064599 (WNT8A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    117064599 (WNT8A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    117064599 (WNT8A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    117064599 (WNT8A)
   05205 Proteoglycans in cancer
    117064599 (WNT8A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    117064599 (WNT8A)
   05226 Gastric cancer
    117064599 (WNT8A)
   05217 Basal cell carcinoma
    117064599 (WNT8A)
   05224 Breast cancer
    117064599 (WNT8A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    117064599 (WNT8A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117064599 (WNT8A)
   05022 Pathways of neurodegeneration - multiple diseases
    117064599 (WNT8A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    117064599 (WNT8A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:tfn00536]
    117064599 (WNT8A)
Glycosaminoglycan binding proteins [BR:tfn00536]
 Heparan sulfate / Heparin
  Morphogens
   117064599 (WNT8A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 117064599
NCBI-ProteinID: XP_033034525
LinkDB
Position
Unknown
AA seq 351 aa
MGNLSMLWAAVGICCAALSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYTITKNCSMGDFENCGCDGSKNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC
KCHGISGSCSIQTCWLQLADFREMGDYLKAKYDQALKIEMDKRQLRAGNSAEGHWAPAEA
FLPSAEAELIFLEESPDYCTCNSSLGIYGTEGRECLQNSHNTSRWERRSCGRLCTECGLQ
VEERKTEVISSCNCKFQWCCKVKCDQCRHVVSKYYCTRSSGSAQSLSEGSA
NT seq 1056 nt   +upstreamnt  +downstreamnt
atggggaacctgtctatgctctgggcagctgtgggcatatgctgtgctgcactcagtgcc
tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctacctgacctacacg
actagcgtggccttgggtgcccagagtggcatcgaggaatgcaagttccagtttgcttgg
gaacgctggaactgccctgaaaatgctcttcagctctctacccacaataggctgagaagt
gccaccagagagacttccttcatacatgctatcagctctgctggagtcatgtacaccatc
accaagaactgtagcatgggtgacttcgaaaactgtggctgtgatgggtcaaaaaatgga
aaaacaggaggccatggctggatctggggaggctgcagtgacaatgtggaatttggggaa
aggatctccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatg
aatcttcacaacaacagggctggcagactggcagtgagagccaccatgaaaaggacctgc
aaatgtcatggcatctctggaagctgcagcatacagacgtgctggctgcagctggctgac
ttccgggagatgggagactacctaaaggccaagtatgaccaggcgctgaaaattgaaatg
gataagcggcagctgagagctgggaacagcgccgagggccactgggcgcccgctgaggcc
ttccttcctagtgcagaggcggaactgatctttttagaggaatcaccagattactgtacc
tgcaattccagcctgggcatctacggcacagagggtcgtgagtgcctacagaacagccac
aacacatccaggtgggagcgacgtagctgtgggcgcctgtgcactgaatgtgggctgcag
gtggaagagaggaaaactgaggtcataagcagctgtaactgcaaattccagtggtgctgt
aaggtcaagtgtgaccagtgtaggcatgtggtaagcaagtattactgcacacgctcctca
ggcagtgcccagtccctgagtgagggcagtgcctga

DBGET integrated database retrieval system