KEGG   Piliocolobus tephrosceles (Ugandan red Colobus): 111529314
Entry
111529314         CDS       T07491                                 
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
pteh  Piliocolobus tephrosceles (Ugandan red Colobus)
Pathway
pteh04150  mTOR signaling pathway
pteh04310  Wnt signaling pathway
pteh04390  Hippo signaling pathway
pteh04550  Signaling pathways regulating pluripotency of stem cells
pteh04916  Melanogenesis
pteh04934  Cushing syndrome
pteh05010  Alzheimer disease
pteh05022  Pathways of neurodegeneration - multiple diseases
pteh05165  Human papillomavirus infection
pteh05200  Pathways in cancer
pteh05205  Proteoglycans in cancer
pteh05217  Basal cell carcinoma
pteh05224  Breast cancer
pteh05225  Hepatocellular carcinoma
pteh05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pteh00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    111529314 (WNT7A)
   04390 Hippo signaling pathway
    111529314 (WNT7A)
   04150 mTOR signaling pathway
    111529314 (WNT7A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    111529314 (WNT7A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    111529314 (WNT7A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    111529314 (WNT7A)
   05205 Proteoglycans in cancer
    111529314 (WNT7A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    111529314 (WNT7A)
   05226 Gastric cancer
    111529314 (WNT7A)
   05217 Basal cell carcinoma
    111529314 (WNT7A)
   05224 Breast cancer
    111529314 (WNT7A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    111529314 (WNT7A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    111529314 (WNT7A)
   05022 Pathways of neurodegeneration - multiple diseases
    111529314 (WNT7A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    111529314 (WNT7A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pteh00536]
    111529314 (WNT7A)
Glycosaminoglycan binding proteins [BR:pteh00536]
 Heparan sulfate / Heparin
  Morphogens
   111529314 (WNT7A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 111529314
NCBI-ProteinID: XP_023051978
Ensembl: ENSPTEG00000011885
UniProt: A0A8C9GYE4
LinkDB
Position
2:47157989..47214518
AA seq 349 aa
MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
IIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKIFVDAREIKQNARTLM
NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP
VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ
ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYTCK
NT seq 1050 nt   +upstreamnt  +downstreamnt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcggtggcttctcctcagtggtagctctgggcgcaagcatcatctgtaacaag
atcccaggcctagctcctagacagcgggcgatctgccagagccggcccgacgccatcatc
atcataggagaaggctcgcaaatgggcctggacgagtgtcagtttcagttccgcaatggc
cgctggaactgctctgcactgggagagcgcactgtcttcgggaaggagctgaaagtgggg
agccgggaggctgcgttcacctacgccatcattgctgccggcgtggcccatgccatcaca
gctgcctgtacccagggcaacctaagcgactgtggctgcgacaaagagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc
ggcttcgccaagatctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttgcacaataacgaggcaggccgaaagatcctggaggagaacatgaagctggaatgt
aagtgccatggcgtgtcaggctcgtgcaccaccaagacgtgctggaccacactgccacag
tttcgggagctgggctacgtgctcaaggacaagtacaacgaggccgttcacgtggagcct
gtgcgtgccagccgcaacaagaggcccaccttcctgaagatcaagaagccactgtcatac
cgcaagcccatggacacggacctggtgtacatcgagaagtcgcccaactactgcgaggag
gacccggtgaccggcagtgtgggcacccagggccgcgcctgcaacaagacggccccccag
gccagcggctgtgacctcatgtgctgtgggcgtggctacaacacccaccagtacgcccgc
gtgtggcagtgcaactgtaagttccactggtgctgttatgtcaagtgcaacacgtgcagc
gagcgcacagagatgtacacgtgcaagtga

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