KEGG   Trachypithecus francoisi (Francois's langur): 117096327
Entry
117096327         CDS       T07225                                 
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
tfn  Trachypithecus francoisi (Francois's langur)
Pathway
tfn04150  mTOR signaling pathway
tfn04310  Wnt signaling pathway
tfn04390  Hippo signaling pathway
tfn04550  Signaling pathways regulating pluripotency of stem cells
tfn04916  Melanogenesis
tfn04934  Cushing syndrome
tfn05010  Alzheimer disease
tfn05022  Pathways of neurodegeneration - multiple diseases
tfn05165  Human papillomavirus infection
tfn05200  Pathways in cancer
tfn05205  Proteoglycans in cancer
tfn05217  Basal cell carcinoma
tfn05224  Breast cancer
tfn05225  Hepatocellular carcinoma
tfn05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:tfn00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    117096327 (WNT7B)
   04390 Hippo signaling pathway
    117096327 (WNT7B)
   04150 mTOR signaling pathway
    117096327 (WNT7B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    117096327 (WNT7B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    117096327 (WNT7B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    117096327 (WNT7B)
   05205 Proteoglycans in cancer
    117096327 (WNT7B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    117096327 (WNT7B)
   05226 Gastric cancer
    117096327 (WNT7B)
   05217 Basal cell carcinoma
    117096327 (WNT7B)
   05224 Breast cancer
    117096327 (WNT7B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    117096327 (WNT7B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    117096327 (WNT7B)
   05022 Pathways of neurodegeneration - multiple diseases
    117096327 (WNT7B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    117096327 (WNT7B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:tfn00536]
    117096327 (WNT7B)
Glycosaminoglycan binding proteins [BR:tfn00536]
 Heparan sulfate / Heparin
  Morphogens
   117096327 (WNT7B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 117096327
NCBI-ProteinID: XP_033089497
LinkDB
Position
Unknown
AA seq 349 aa
MHRNFRKWIFYVFLCFGVLYVKLGALSSVVALGANIICNKIPGLAPRQRAICQSRPDAII
VIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHAVT
AACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARRLM
NLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAVQVEV
VRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPG
ADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq 1050 nt   +upstreamnt  +downstreamnt
atgcacagaaactttcgcaagtggattttctacgtgtttctctgctttggcgtcctgtac
gtgaagctcggagcactgtcatcagtggtggccctgggagccaacatcatctgcaacaag
attcctggcctagccccgcggcagcgtgccatctgccagagccggcccgatgccatcatt
gtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccagttccgctttgga
cgctggaactgctctgccctcggcgagaagactgtctttgggcaagagctccgagtaggg
agccgtgaggctgccttcacgtatgccatcaccgcggctggtgtagcgcacgccgtcact
gctgcctgcagccaaggcaacctgagcaactgcggctgtgaccgcgagaagcagggttac
tacaaccaggccgagggctggaagtggggtggctgctcagccgacgtgcgttacggcatc
gacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcgcggcgcctcatg
aacctgcacaacaatgaggccggcaggaaggttctggaggaccggatgcagctggagtgc
aagtgtcacggtgtgtctggctcctgcaccaccaagacctgctggaccacgctgcccaag
tttcgagaggtgggccacctgctgaaggagaagtacaacgcggctgtgcaggtggaggtg
gtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaaacagctgcgcagctat
cagaagcccatggagacggacctggtgtacatcgagaagtcgcccaactactgcgaggag
gacgcggccacgggcagcgtgggcacgcagggccgcctctgcaaccgcacgtcgcccggt
gcggacggctgtgacaccatgtgctgcggccgaggctacaacacccaccagtacaccaag
gtgtggcagtgcaactgcaaattccactggtgctgcttcgtcaagtgcaacacctgcagc
gagcgcaccgaggtcttcacctgcaagtga

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