KEGG   Pteropus alecto (black flying fox): 102888597
Entry
102888597         CDS       T02993                                 
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
pale  Pteropus alecto (black flying fox)
Pathway
pale04150  mTOR signaling pathway
pale04310  Wnt signaling pathway
pale04390  Hippo signaling pathway
pale04550  Signaling pathways regulating pluripotency of stem cells
pale04916  Melanogenesis
pale04934  Cushing syndrome
pale05010  Alzheimer disease
pale05022  Pathways of neurodegeneration - multiple diseases
pale05165  Human papillomavirus infection
pale05200  Pathways in cancer
pale05205  Proteoglycans in cancer
pale05217  Basal cell carcinoma
pale05224  Breast cancer
pale05225  Hepatocellular carcinoma
pale05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pale00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    102888597 (WNT7A)
   04390 Hippo signaling pathway
    102888597 (WNT7A)
   04150 mTOR signaling pathway
    102888597 (WNT7A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    102888597 (WNT7A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    102888597 (WNT7A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    102888597 (WNT7A)
   05205 Proteoglycans in cancer
    102888597 (WNT7A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    102888597 (WNT7A)
   05226 Gastric cancer
    102888597 (WNT7A)
   05217 Basal cell carcinoma
    102888597 (WNT7A)
   05224 Breast cancer
    102888597 (WNT7A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    102888597 (WNT7A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102888597 (WNT7A)
   05022 Pathways of neurodegeneration - multiple diseases
    102888597 (WNT7A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    102888597 (WNT7A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pale00536]
    102888597 (WNT7A)
Glycosaminoglycan binding proteins [BR:pale00536]
 Heparan sulfate / Heparin
  Morphogens
   102888597 (WNT7A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 102888597
NCBI-ProteinID: XP_006917506
LinkDB
Position
Unknown
AA seq 349 aa
MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP
VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ
ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEVYTCK
NT seq 1050 nt   +upstreamnt  +downstreamnt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcggtggcttctcctcggtggtagctctgggcgcgagcatcatctgtaacaag
atcccaggcctggctcccagacagcgggcgatctgccagagccggcccgacgccatcatc
gtcataggagaaggctcacaaatgggcctcgacgagtgtcagtttcagttccgcaatggc
cgctggaactgctccgcgctgggggagcgcaccgtcttcggaaaggagctcaaagtgggg
agccgagaggctgccttcacgtatgccatcattgctgccggtgtggcccatgccatcaca
gctgcctgtacccagggcaacctgagtgactgtggctgcgacaaggagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacattcgctacggcatc
ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttacacaataacgaggcaggccgaaagatcctggaagagaacatgaagctggagtgt
aagtgccatggcgtgtcagggtcatgcaccaccaagacgtgctggaccacactgccacag
ttccgggagctgggctatgtgctcaaggacaagtacaatgaggctgttcacgtggagcct
gtacgcgctagccgcaacaagcggcccaccttcctgaagatcaagaagccactgtcatac
cgcaagcccatggacacagacctggtgtacatcgagaagtcacccaactactgtgaggag
gacccagtgaccggtagtgtgggcacgcagggccgcgcctgcaacaagacagccccccaa
gccagtggttgtgacctcatgtgctgtggccgtggctacaacacccaccagtatgcccgc
gtgtggcagtgcaactgcaaattccactggtgctgctatgtcaagtgcaacacctgcagt
gaacgcacggaagtgtatacgtgcaagtga

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