KEGG   Macaca fascicularis (crab-eating macaque): 102135636
Entry
102135636         CDS       T02918                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X2
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
mcf  Macaca fascicularis (crab-eating macaque)
Pathway
mcf04150  mTOR signaling pathway
mcf04310  Wnt signaling pathway
mcf04390  Hippo signaling pathway
mcf04550  Signaling pathways regulating pluripotency of stem cells
mcf04916  Melanogenesis
mcf04934  Cushing syndrome
mcf05010  Alzheimer disease
mcf05022  Pathways of neurodegeneration - multiple diseases
mcf05165  Human papillomavirus infection
mcf05200  Pathways in cancer
mcf05205  Proteoglycans in cancer
mcf05217  Basal cell carcinoma
mcf05224  Breast cancer
mcf05225  Hepatocellular carcinoma
mcf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mcf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102135636 (WNT7B)
   04390 Hippo signaling pathway
    102135636 (WNT7B)
   04150 mTOR signaling pathway
    102135636 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102135636 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102135636 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102135636 (WNT7B)
   05205 Proteoglycans in cancer
    102135636 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102135636 (WNT7B)
   05226 Gastric cancer
    102135636 (WNT7B)
   05217 Basal cell carcinoma
    102135636 (WNT7B)
   05224 Breast cancer
    102135636 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102135636 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102135636 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    102135636 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102135636 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mcf00536]
    102135636 (WNT7B)
Glycosaminoglycan binding proteins [BR:mcf00536]
 Heparan sulfate / Heparin
  Morphogens
   102135636 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102135636
NCBI-ProteinID: XP_005567064
Ensembl: ENSMFAG00000043981
LinkDB
Position
10:join(5614252..5614322,5640794..5641020,5659463..5659734,5667286..5667765)
AA seq 349 aa
MHRNFRKWIFYVFLCFGVLYVKLGALSSVVALGANIICNKIPGLAPRQRAICQSRPDAII
VIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHAVT
AACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARRLM
NLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAVQVEV
VRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPG
ADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1050 nt   +upstreamnt  +downstreamnt
atgcacagaaactttcgcaagtggattttctacgtgtttctctgctttggcgtcctgtac
gtgaagctcggagcactgtcatcagtggtggccctgggagccaacatcatctgcaacaag
attcctggcctagccccgcggcagcgtgccatctgccagagccggcccgatgccatcatt
gtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccagttccgctttgga
cgctggaactgctctgccctcggcgagaagactgtctttgggcaagagctccgagtaggg
agccgtgaggctgccttcacgtatgccatcaccgcggctggcgtagcacacgccgtcact
gctgcctgcagccaaggcaacctgagcaactgcggctgtgaccgagagaagcagggctac
tacaaccaggccgagggctggaagtggggtggctgctcggctgacgtgcgttacggcatc
gacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcgcggcgcctcatg
aacctgcacaacaatgaggccggcaggaaggttctggaggaccgaatgcagctggagtgc
aagtgtcacggcgtgtctggctcctgcaccaccaagacctgctggaccacgctgcccaag
ttccgagaggtgggccacctgctgaaggagaagtacaacgcggccgtgcaggtggaggtg
gtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaaacagctgcgcagctat
cagaagcccatggagacggacctggtgtacatcgagaagtcacccaactactgcgaggag
gacgcggccacgggcagcgtgggcacgcagggccgcctctgcaaccgcacgtcgcccggt
gcggacggctgtgacaccatgtgctgtggccgaggctacaacacccaccagtacaccaag
gtgtggcagtgcaactgcaaattccactggtgctgcttcgtcaagtgcaacacctgcagc
gagcgcaccgaggtcttcacctgcaagtga

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