KEGG   Gorilla gorilla gorilla (western lowland gorilla): 115931954
Entry
115931954         CDS       T02442                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X2
  KO
K00572  wingless-type MMTV integration site family, member 7
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
    115931954 (WNT7B)
   04390 Hippo signaling pathway
    115931954 (WNT7B)
   04150 mTOR signaling pathway
    115931954 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    115931954 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    115931954 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    115931954 (WNT7B)
   05205 Proteoglycans in cancer
    115931954 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    115931954 (WNT7B)
   05226 Gastric cancer
    115931954 (WNT7B)
   05217 Basal cell carcinoma
    115931954 (WNT7B)
   05224 Breast cancer
    115931954 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    115931954 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    115931954 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    115931954 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    115931954 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ggo00536]
    115931954 (WNT7B)
Glycosaminoglycan binding proteins [BR:ggo00536]
 Heparan sulfate / Heparin
  Morphogens
   115931954 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 115931954
NCBI-ProteinID: XP_030861497
LinkDB
Position
23:complement(join(43933484..43933963,43941268..43941539,43959924..43960150,43986554..43986624))
AA seq 349 aa
MHRNFRKWIFYVFLCFGVLYVKLGALSSVVALGANIICNKIPGLAPRQRAICQSRPDAII
VIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHAVT
AACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARRLM
NLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAVQVEV
VRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPG
ADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1050 nt   +upstreamnt  +downstreamnt
atgcacagaaactttcgcaagtggattttctacgtgtttctctgctttggcgtcctgtac
gtgaagctcggagcactgtcatccgtggtggccctgggagccaacatcatctgcaacaag
attcctggcctagccccgcggcagcgtgccatctgccagagccggcccgatgccatcatt
gtgattggggagggggcgcagatgggcatcaacgagtgccagtaccagttccgcttcgga
cgctggaactgctctgccctcggcgagaagactgtcttcgggcaagagctccgagtaggg
agccgtgaggctgccttcacgtacgccatcaccgcggctggcgtagcgcacgccgtcacc
gctgcctgcagccaaggcaacctgagcaactgcggctgcgaccgcgagaagcagggctac
tacaaccaagccgagggctggaagtggggcggctgctcggccgacgtgcgttacggcatc
gacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcgcggcgcctcatg
aacctgcataacaatgaggccggcaggaaggttctagaggaccggatgcagctggagtgc
aagtgccacggcgtgtctggctcctgcaccaccaaaacctgctggaccacgctgcccaag
ttccgagaggtgggccacctgctgaaggagaagtacaacgcggccgtgcaggtggaggtg
gtgcgggccagccgtctgcggcagcccaccttcctgcgcatcaaacagctgcgcagctat
cagaagcccatggagacagacctggtgtacattgagaagtcgcccaactactgcgaggag
gacgcggccacgggcagcgtgggcacgcagggccgtctctgcaaccgcacgtcgcccggc
gcggacggctgtgacaccatgtgctgcggccgaggctacaacacccaccagtacaccaag
gtgtggcagtgcaactgcaaattccactggtgctgctttgtcaagtgcaacacctgcagc
gagcgcaccgaggtcttcacctgcaagtga

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