KEGG   Piliocolobus tephrosceles (Ugandan red Colobus): 111553419
Entry
111553419         CDS       T07491                                 
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
  KO
K00182  wingless-type MMTV integration site family, member 2
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
    111553419 (WNT2)
   04390 Hippo signaling pathway
    111553419 (WNT2)
   04150 mTOR signaling pathway
    111553419 (WNT2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    111553419 (WNT2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    111553419 (WNT2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    111553419 (WNT2)
   05205 Proteoglycans in cancer
    111553419 (WNT2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    111553419 (WNT2)
   05226 Gastric cancer
    111553419 (WNT2)
   05217 Basal cell carcinoma
    111553419 (WNT2)
   05224 Breast cancer
    111553419 (WNT2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    111553419 (WNT2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    111553419 (WNT2)
   05022 Pathways of neurodegeneration - multiple diseases
    111553419 (WNT2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    111553419 (WNT2)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pteh00536]
    111553419 (WNT2)
Glycosaminoglycan binding proteins [BR:pteh00536]
 Heparan sulfate / Heparin
  Morphogens
   111553419 (WNT2)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 111553419
NCBI-ProteinID: XP_023083985
Ensembl: ENSPTEG00000024005
UniProt: A0A8C9HPN1
LinkDB
Position
8:complement(109852529..109898602)
AA seq 360 aa
MNAPLGGIWLWLPLLLTWLTPEVNSSWWYMRATGGSSRVMCDNVPGLVSSQRQLCHRHPD
VMRAISQGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVV
FAITRACSQGEVKSCSCDPKKMGSAKDSKGIFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG
AIQVVMNQDGTGFTVANERFKKPTKNDLVYFENSPDYCIRDREAGSLGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSHVTRMTKCGCKFHWCCAVRCQDCLEALDVHTCKAPKNADWTTPT
NT seq 1083 nt   +upstreamnt  +downstreamnt
atgaacgcccctctcggtggaatctggctctggctccctctgctcttgacctggctcacc
cccgaggtcaactcttcatggtggtacatgagagctacaggtggctcctccagggtgatg
tgcgataatgtgccaggcctggtgagcagccagcggcagctgtgtcaccgacatccagat
gtgatgcgtgccattagccagggcgtggccgagtggacagcggaatgccagcaccagttc
cgccagcaccgctggaattgcaacactctggacagggatcacagcctctttggcagggtc
ctactccgaagtagtcgggaatctgcctttgtttatgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaagtaaaatcctgttcctgtgatccaaag
aagatgggaagcgccaaggacagcaagggcatttttgattggggtggctgcagtgataac
attgactatgggatcaaatttgcccgcgcattcgtggatgccaaggaaaggaaaggaaag
gatgccagagccctgatgaatcttcataacaacagagctggcaggaaggctgtaaagcgg
ttcttgaaacaagagtgcaaatgccatggggtgagcggctcgtgtactctcaggacatgc
tggctggccatggccgacttcaggaaaacgggcgattatctctggaggaagtacaatggg
gccatccaggtggtcatgaaccaggatggcacaggtttcactgtggctaacgagaggttt
aagaagccaacaaaaaatgacctcgtgtattttgagaattctccagactactgtatcagg
gaccgagaggcaggctccctgggtacagcaggccgagtgtgcaacctgacttcccggggc
atggacagctgcgaagtcatgtgctgtgggagaggctacgacacctcccatgtcacccgg
atgaccaagtgtggatgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg
gaggccctggacgtgcacacatgcaaggcccccaagaacgctgactggacaacccccaca
tga

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