KEGG   Piliocolobus tephrosceles (Ugandan red Colobus): 111538807
Entry
111538807         CDS       T07491                                 
Symbol
WNT8B
Name
(RefSeq) protein Wnt-8b
  KO
K00714  wingless-type MMTV integration site family, member 8
Organism
pteh  Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04150  mTOR signaling pathway
pteh04310  Wnt signaling pathway
pteh04390  Hippo signaling pathway
pteh04550  Signaling pathways regulating pluripotency of stem cells
pteh04916  Melanogenesis
pteh04934  Cushing syndrome
pteh05010  Alzheimer disease
pteh05022  Pathways of neurodegeneration - multiple diseases
pteh05165  Human papillomavirus infection
pteh05200  Pathways in cancer
pteh05205  Proteoglycans in cancer
pteh05217  Basal cell carcinoma
pteh05224  Breast cancer
pteh05225  Hepatocellular carcinoma
pteh05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pteh00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    111538807 (WNT8B)
   04390 Hippo signaling pathway
    111538807 (WNT8B)
   04150 mTOR signaling pathway
    111538807 (WNT8B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    111538807 (WNT8B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    111538807 (WNT8B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    111538807 (WNT8B)
   05205 Proteoglycans in cancer
    111538807 (WNT8B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    111538807 (WNT8B)
   05226 Gastric cancer
    111538807 (WNT8B)
   05217 Basal cell carcinoma
    111538807 (WNT8B)
   05224 Breast cancer
    111538807 (WNT8B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    111538807 (WNT8B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    111538807 (WNT8B)
   05022 Pathways of neurodegeneration - multiple diseases
    111538807 (WNT8B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    111538807 (WNT8B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pteh00536]
    111538807 (WNT8B)
Glycosaminoglycan binding proteins [BR:pteh00536]
 Heparan sulfate / Heparin
  Morphogens
   111538807 (WNT8B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 111538807
NCBI-ProteinID: XP_023062197
Ensembl: ENSPTEG00000028100
UniProt: A0A8C9I605
LinkDB
Position
9:complement(33238846..33263042)
AA seq 351 aa
MFLSKPSVYISLFTCVLQLSHSWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAW
DRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNG
QLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTC
KCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRS
ISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEE
RRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRKP
NT seq 1056 nt   +upstreamnt  +downstreamnt
atgtttctttcaaagccttctgtgtacatctctcttttcacctgtgtcctccaactcagc
cacagctggtcagtgaacaatttcctgatgactggtccaaaggcttacctgatttactcc
agcagtgtggcagctggtgcccagagtggtattgaagaatgcaagtatcagtttgcctgg
gaccgctggaactgccctgagagagctctgcagctgtccagccatggtgggcttcgcagt
gctaatcgggagacagcatttgtgcatgccatcagttctgctggagtcatgtacaccctg
actagaaactgcagccttggagattttgataactgtggctgtgatgactcccgcaatggg
caactggggggccaaggctggctgtggggaggctgcagcgacaatgtgggcttcggagag
gcgatttccaagcagtttgtcgatgccctggaaacaggacaggatgcacgggcagccatg
aacctgcacaacaacgaggctggccgcaaggcggtgaagggcaccatgaaacgtacgtgc
aagtgccacggcgtgtctggcagctgcaccacgcagacctgttggttgcagctgcccgag
ttccgcgaggtgggcgcgcacctaaaggagaagtaccacgcagcactcaaggtagacctg
ctgcagggtgctggcaacagcgctgccggccgcggcgccatcgccgacacctttcgctcc
atctccacccgggagctggtgcacctggaggactccccggactactgcctggagaacaaa
acgctaggactgctgggcaccgaaggccgagagtgcctgaggcgcgggcgggccctgggt
cgctgggaacgccgcagctgccgccggctctgcggggactgcgggctggcggtggaggag
cgccgggccgagaccgtgtccagctgcaactgcaagttccactggtgctgcgcagtccgc
tgcgagcagtgccgccggcgggtcaccaagtacttctgcagccgcgcagagcggccgcgg
gggggcgctgcgcacaaacccgggagaaaaccctaa

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