KEGG   Rousettus aegyptiacus (Egyptian rousette): 107505364
Entry
107505364         CDS       T06036                                 
Symbol
WNT2
Name
(RefSeq) protein Wnt-2 isoform X4
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
ray  Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04150  mTOR signaling pathway
ray04310  Wnt signaling pathway
ray04390  Hippo signaling pathway
ray04550  Signaling pathways regulating pluripotency of stem cells
ray04916  Melanogenesis
ray04934  Cushing syndrome
ray05010  Alzheimer disease
ray05022  Pathways of neurodegeneration - multiple diseases
ray05165  Human papillomavirus infection
ray05200  Pathways in cancer
ray05205  Proteoglycans in cancer
ray05217  Basal cell carcinoma
ray05224  Breast cancer
ray05225  Hepatocellular carcinoma
ray05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ray00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    107505364 (WNT2)
   04390 Hippo signaling pathway
    107505364 (WNT2)
   04150 mTOR signaling pathway
    107505364 (WNT2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    107505364 (WNT2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    107505364 (WNT2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    107505364 (WNT2)
   05205 Proteoglycans in cancer
    107505364 (WNT2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    107505364 (WNT2)
   05226 Gastric cancer
    107505364 (WNT2)
   05217 Basal cell carcinoma
    107505364 (WNT2)
   05224 Breast cancer
    107505364 (WNT2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    107505364 (WNT2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    107505364 (WNT2)
   05022 Pathways of neurodegeneration - multiple diseases
    107505364 (WNT2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    107505364 (WNT2)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ray00536]
    107505364 (WNT2)
Glycosaminoglycan binding proteins [BR:ray00536]
 Heparan sulfate / Heparin
  Morphogens
   107505364 (WNT2)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 107505364
NCBI-ProteinID: XP_015990958
LinkDB
Position
Unknown
AA seq 482 aa
MRRSSSSPPPARTHISGSPRRASQAGGGLLRPRKRAVEQFTAAASSWSSFLSGDKRRGCK
PIAAQDAPPAGASLSLSPLCRGPDPGRRRSFCLHKAQRLRARAAGGATHGRLFAASVPPS
VIFCAPQRWGGAGCASKPHLPRTLWPGTPGYMKATGGSSRVMCDNVPGLVSRQRQLCHRH
PDVMRAIGLGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAG
VVFAITRACSQGELKSCSCDPKKKGTAKDSKGTFDWGGCSDNIDYGIKFARAFVDAKERK
GKDARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKY
NGAIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDRDAGSLGTAGRVCNLTS
RGMDSCEVMCCGRGYDTSRVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPKSADWAA
TT
NT seq 1449 nt   +upstreamnt  +downstreamnt
atgcggcgctcgtcttcatccccgcccccagcacgcacacacatttcgggttccccaagg
cgtgcttcccaggcgggcggcgggctcctccgccctaggaaaagagcagtggaacagttc
acggccgccgcgagttcctggtcttccttcctttccggtgataaacggcggggctgcaag
ccaattgctgctcaagatgctccacccgcgggcgcgagcctctctctctctccgctctgc
aggggcccagatccaggacggagaaggtccttttgcctccacaaagctcaaaggctgaga
gccagggcggcgggaggcgcgacccacggcaggctcttcgctgcctcggtgcctccctcc
gtgatcttttgcgctccacagcgttggggaggagctgggtgtgcgtcaaaaccgcatctt
ccccggacgctttggccagggacgcctgggtacatgaaagcgacaggcggctcctccagg
gtgatgtgcgacaatgtgccagggctggtgagccgccagcggcagctgtgccaccgacac
ccagatgtgatgcgtgccattggcctgggtgtggccgagtggacggccgagtgccagcac
cagttccgccagcaccgctggaactgcaacaccctggacagggaccacagcctctttggc
agagtcctgctccgaagtagtcgggaatctgcctttgtttacgccatctcctcagctgga
gttgtatttgccatcaccagggcctgtagccaaggagaattaaaatcctgttcctgtgat
ccaaagaagaagggaaccgccaaggacagcaagggcactttcgactggggtggctgcagt
gataacattgactatgggatcaaatttgctcgagcgtttgtggatgccaaggaaaggaaa
ggaaaggacgccagagccctgatgaatctgcacaacaacagagctggccggaaggctgta
aagaggtttttgaaacaagagtgcaagtgtcacggcgtgagcggctcatgcaccctgcgg
acatgctggctggccatggccgacttcagaaaaacgggtgattatctgtggaggaagtac
aacggggccatccaggtcgtcatgaaccaggacggcactggctttactgtggctaacaag
aggtttaagaagccaacgaaaaacgacctcgtgtattttgagaattctccagactactgt
atcagggaccgagatgcaggctccctgggtacagcaggacgtgtgtgcaacctgacctcc
cgaggcatggacagctgtgaagtcatgtgctgcgggagaggctacgacacctcccgcgtc
acgaggatgaccaagtgtgagtgtaagttccactggtgctgtgctgtccgctgtcaggac
tgcctggaggccctggacgtgcacacgtgcaaggcacctaagagtgccgactgggcggct
accacatga

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