KEGG   Rhinopithecus roxellana (golden snub-nosed monkey): 104681717
Entry
104681717         CDS       T03989                                 
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a isoform X1
  KO
K00714  wingless-type MMTV integration site family, member 8
Organism
rro  Rhinopithecus roxellana (golden snub-nosed monkey)
Pathway
rro04150  mTOR signaling pathway
rro04310  Wnt signaling pathway
rro04390  Hippo signaling pathway
rro04550  Signaling pathways regulating pluripotency of stem cells
rro04916  Melanogenesis
rro04934  Cushing syndrome
rro05010  Alzheimer disease
rro05022  Pathways of neurodegeneration - multiple diseases
rro05165  Human papillomavirus infection
rro05200  Pathways in cancer
rro05205  Proteoglycans in cancer
rro05217  Basal cell carcinoma
rro05224  Breast cancer
rro05225  Hepatocellular carcinoma
rro05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:rro00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    104681717 (WNT8A)
   04390 Hippo signaling pathway
    104681717 (WNT8A)
   04150 mTOR signaling pathway
    104681717 (WNT8A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    104681717 (WNT8A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    104681717 (WNT8A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    104681717 (WNT8A)
   05205 Proteoglycans in cancer
    104681717 (WNT8A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    104681717 (WNT8A)
   05226 Gastric cancer
    104681717 (WNT8A)
   05217 Basal cell carcinoma
    104681717 (WNT8A)
   05224 Breast cancer
    104681717 (WNT8A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    104681717 (WNT8A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    104681717 (WNT8A)
   05022 Pathways of neurodegeneration - multiple diseases
    104681717 (WNT8A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    104681717 (WNT8A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:rro00536]
    104681717 (WNT8A)
Glycosaminoglycan binding proteins [BR:rro00536]
 Heparan sulfate / Heparin
  Morphogens
   104681717 (WNT8A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 104681717
NCBI-ProteinID: XP_010386378
LinkDB
Position
3:154721310..154729989
AA seq 355 aa
MGSLSMLWAAVGICCAALSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYTITKNCSMGDFENCGCDGSKNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC
KCHGISGSCSIQTCWLQLADFREMGDYLKAKYDQALKIEMDKRQLRAGNSAEGHWAPAEA
FLPSAEAELIFLEESPDYCTCNSSLGIYGTEGRECLQNSHNTSRWERRSCGRLCTECGLQ
VEERKTEVISSCNCKFQWCCKVKCDQCRHVVSKYYCTRSSGSAQSLRRVWFGVHI
NT seq 1068 nt   +upstreamnt  +downstreamnt
atggggagcctgtctatgctctgggcagctgtgggcatatgctgtgctgcactcagcgcc
tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctacctgacctacacg
actagcgtggccttgggtgcccagagtggcatcgaggaatgcaagttccagtttgcttgg
gaacgctggaactgccctgaaaatgctcttcagctctctacccacaataggctgagaagt
gccaccagagagacttccttcatacatgctatcagctctgctggagtcatgtacaccatc
accaagaactgtagcatgggtgacttcgaaaactgtggctgtgatgggtcaaaaaatgga
aaaacaggaggccatggctggatctggggaggctgcagtgacaatgtggaatttggggaa
aggatctccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatg
aatcttcacaacaacagggccggcagactggcagtgagagccaccatgaaaaggacctgc
aaatgtcatggcatctctggaagctgcagcatacagacgtgctggctgcagctggctgac
ttccgggagatgggagactacctaaaggccaagtatgaccaggcgctgaaaattgaaatg
gataagcggcagctgagagctgggaacagcgccgagggccactgggcgcccgctgaggcc
ttccttcctagtgcagaggcggaactgatctttttagaggaatcaccagattactgtacc
tgcaattccagcctgggcatctatggcacagagggtcgtgagtgcctacagaacagccac
aacacatccaggtgggagcgacgtagctgtgggcgcctgtgcactgaatgtgggctgcag
gtggaagagaggaaaactgaggtcataagtagctgtaactgcaaattccagtggtgctgt
aaggtcaagtgtgaccagtgtaggcatgtggtgagcaagtattactgcacacgctcctca
ggcagtgcccagtccctgaggagagtttggtttggggtccatatctag

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