KEGG   Gorilla gorilla gorilla (western lowland gorilla): 101130779
Entry
101130779         CDS       T02442                                 
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
ggo  Gorilla gorilla gorilla (western lowland gorilla)
Pathway
ggo04150  mTOR signaling pathway
ggo04310  Wnt signaling pathway
ggo04390  Hippo signaling pathway
ggo04550  Signaling pathways regulating pluripotency of stem cells
ggo04916  Melanogenesis
ggo04934  Cushing syndrome
ggo05010  Alzheimer disease
ggo05022  Pathways of neurodegeneration - multiple diseases
ggo05165  Human papillomavirus infection
ggo05200  Pathways in cancer
ggo05205  Proteoglycans in cancer
ggo05217  Basal cell carcinoma
ggo05224  Breast cancer
ggo05225  Hepatocellular carcinoma
ggo05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ggo00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101130779 (WNT2)
   04390 Hippo signaling pathway
    101130779 (WNT2)
   04150 mTOR signaling pathway
    101130779 (WNT2)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101130779 (WNT2)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101130779 (WNT2)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101130779 (WNT2)
   05205 Proteoglycans in cancer
    101130779 (WNT2)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101130779 (WNT2)
   05226 Gastric cancer
    101130779 (WNT2)
   05217 Basal cell carcinoma
    101130779 (WNT2)
   05224 Breast cancer
    101130779 (WNT2)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101130779 (WNT2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101130779 (WNT2)
   05022 Pathways of neurodegeneration - multiple diseases
    101130779 (WNT2)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101130779 (WNT2)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ggo00536]
    101130779 (WNT2)
Glycosaminoglycan binding proteins [BR:ggo00536]
 Heparan sulfate / Heparin
  Morphogens
   101130779 (WNT2)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 101130779
NCBI-ProteinID: XP_004046149
Ensembl: ENSGGOG00000009721
UniProt: Q2IBF4
Position
7:complement(109436081..109482210)
AA seq 360 aa
MNAPLGGIWLWLPLLLTWLTPEVNSSWWYMRATGGSSRVMCDNVPGLVSSQRQLCHRHPD
VMRAISQGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVV
FAITRACSQGEVKSCSCDPKKMGSAKDSKGIFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG
AIQVVMNQDGTGFTVANERFKKPTKNDLVYFENSPDYCIRDREAGSLGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSHVTRMTKCGCKFHWCCAVRCQDCLEALDVHTCKAPKNADWTTPT
NT seq 1083 nt   +upstreamnt  +downstreamnt
atgaacgcccctctcggtggaatctggctctggctccctctgctcttgacctggctcacc
cccgaggtcaactcttcatggtggtacatgagagctacaggtggctcctccagggtgatg
tgcgataatgtgccaggcctggtgagcagccagcggcagctgtgtcatcgacatccagat
gtgatgcgtgccattagccagggcgtggccgagtggacagcagaatgccagcaccagttc
cgccagcaccgctggaattgcaacaccctggacagggatcacagcctctttggcagggtc
ctactccgaagtagtcgggaatctgcctttgtttatgccatctcctcagctggagttgta
tttgccatcactagggcctgtagccaaggagaagtaaaatcctgttcctgtgatccaaag
aagatgggaagcgccaaggacagcaaaggcatttttgattggggtggctgcagtgataac
attgactatgggatcaaatttgcccgcgcatttgtggatgcaaaggaaaggaaaggaaag
gatgccagagccctgatgaatcttcacaacaacagagctggcaggaaggctgtaaagcgg
ttcttgaaacaagagtgcaagtgccacggggtgagcggctcatgtactctcaggacatgc
tggctggccatggccgacttcaggaaaacgggcgattatctctggaggaagtacaatggg
gccatccaggtggtcatgaaccaggatggcacaggtttcactgtggctaacgagaggttt
aagaagccaacaaaaaatgacctcgtgtattttgagaattctccagactactgtatcagg
gaccgagaggcaggctccctgggtacagcaggccgtgtgtgcaacctgacttcccggggc
atggacagctgtgaagtcatgtgctgtgggagaggctacgacacctcccatgtcacccgg
atgaccaagtgtgggtgtaagttccactggtgctgcgccgtgcgctgtcaggactgcctg
gaagctctggatgtgcacacatgcaaggccccaaagaacgctgactggacaacccctaca
tga

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