KEGG   Microcebus murinus (gray mouse lemur): 105864522
Entry
105864522         CDS       T07238                                 
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a isoform X1
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
mmur  Microcebus murinus (gray mouse lemur)
Pathway
mmur04150  mTOR signaling pathway
mmur04310  Wnt signaling pathway
mmur04390  Hippo signaling pathway
mmur04550  Signaling pathways regulating pluripotency of stem cells
mmur04916  Melanogenesis
mmur04934  Cushing syndrome
mmur05010  Alzheimer disease
mmur05022  Pathways of neurodegeneration - multiple diseases
mmur05165  Human papillomavirus infection
mmur05200  Pathways in cancer
mmur05205  Proteoglycans in cancer
mmur05217  Basal cell carcinoma
mmur05224  Breast cancer
mmur05225  Hepatocellular carcinoma
mmur05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mmur00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    105864522 (WNT7A)
   04390 Hippo signaling pathway
    105864522 (WNT7A)
   04150 mTOR signaling pathway
    105864522 (WNT7A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    105864522 (WNT7A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    105864522 (WNT7A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    105864522 (WNT7A)
   05205 Proteoglycans in cancer
    105864522 (WNT7A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    105864522 (WNT7A)
   05226 Gastric cancer
    105864522 (WNT7A)
   05217 Basal cell carcinoma
    105864522 (WNT7A)
   05224 Breast cancer
    105864522 (WNT7A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    105864522 (WNT7A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    105864522 (WNT7A)
   05022 Pathways of neurodegeneration - multiple diseases
    105864522 (WNT7A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    105864522 (WNT7A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mmur00536]
    105864522 (WNT7A)
Glycosaminoglycan binding proteins [BR:mmur00536]
 Heparan sulfate / Heparin
  Morphogens
   105864522 (WNT7A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 105864522
NCBI-ProteinID: XP_012607912
Ensembl: ENSMICG00000034657
UniProt: A0A8B7FIQ8
LinkDB
Position
23:12491291..12550822
AA seq 349 aa
MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP
VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ
ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYTCK
NT seq 1050 nt   +upstreamnt  +downstreamnt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcgggggcttctcctcagtggtagctctgggcgcaagcatcatctgtaacaag
atcccaggcctggctcccagacagcgggcgatctgccagagccggcccgacgccatcatc
gtcattggagaaggttcgcaaatgggcctggacgagtgtcagtttcagttccgcaatggc
cgctggaactgctctgcactgggggagcgcaccgtctttgggaaggagctcaaagtgggt
agccgggaggctgccttcacctacgccatcattgccgccggcgtggcccacgccatcaca
gctgcctgtacccagggtaacctcagcgactgcggctgcgacaaagagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc
ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttgcacaataacgaggcgggccgaaagatcctggaggagaacatgaagctggaatgt
aagtgccacggcgtgtcaggctcatgcaccaccaagacgtgctggactacactgccgcag
tttcgggagctgggctatgtgctcaaggacaagtacaacgaggctgttcatgtggagccc
gtgcgcgccagccgcaacaagcggcccaccttcctgaagatcaagaagccactgtcttac
cgcaagcccatggacacggacctggtatacatcgaaaagtcacccaactactgcgaggag
gacccagtgacgggcagtgtgggcacacaaggccgtgcctgcaacaagacggccccccag
gccagcggctgtgacctcatgtgctgtggccgtggctacaacacccaccagtatgcccgt
gtgtggcagtgcaactgtaagttccactggtgctgctacgtcaagtgcaacacctgcagc
gagcgcaccgagatgtacacgtgcaaatga

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