KEGG   Mustela nigripes (black-footed ferret): 132009901
Entry
132009901         CDS       T09425                                 
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
  KO
K00572  wingless-type MMTV integration site family, member 7
Organism
mnp  Mustela nigripes (black-footed ferret)
Pathway
mnp04150  mTOR signaling pathway
mnp04310  Wnt signaling pathway
mnp04390  Hippo signaling pathway
mnp04550  Signaling pathways regulating pluripotency of stem cells
mnp04916  Melanogenesis
mnp04934  Cushing syndrome
mnp05010  Alzheimer disease
mnp05022  Pathways of neurodegeneration - multiple diseases
mnp05165  Human papillomavirus infection
mnp05200  Pathways in cancer
mnp05205  Proteoglycans in cancer
mnp05217  Basal cell carcinoma
mnp05224  Breast cancer
mnp05225  Hepatocellular carcinoma
mnp05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mnp00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    132009901 (WNT7A)
   04390 Hippo signaling pathway
    132009901 (WNT7A)
   04150 mTOR signaling pathway
    132009901 (WNT7A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    132009901 (WNT7A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    132009901 (WNT7A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    132009901 (WNT7A)
   05205 Proteoglycans in cancer
    132009901 (WNT7A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    132009901 (WNT7A)
   05226 Gastric cancer
    132009901 (WNT7A)
   05217 Basal cell carcinoma
    132009901 (WNT7A)
   05224 Breast cancer
    132009901 (WNT7A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    132009901 (WNT7A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    132009901 (WNT7A)
   05022 Pathways of neurodegeneration - multiple diseases
    132009901 (WNT7A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    132009901 (WNT7A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mnp00536]
    132009901 (WNT7A)
Glycosaminoglycan binding proteins [BR:mnp00536]
 Heparan sulfate / Heparin
  Morphogens
   132009901 (WNT7A)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 132009901
NCBI-ProteinID: XP_059243906
LinkDB
Position
2:55958273..56018895
AA seq 349 aa
MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP
VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ
ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEVYTCK
NT seq 1050 nt   +upstreamnt  +downstreamnt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcggtggcttctcctcggtggtagctctgggcgcgagcatcatctgtaacaag
atcccgggcctagctcccagacagcgggcaatctgccagagccgacccgacgccatcatc
gtcataggagaaggctcacaaatgggtctcgacgagtgtcagtttcagttccgcaatggc
cgctggaactgctcagcactaggggagcgcaccgtcttcgggaaggagctcaaagtgggg
agccgggaggctgccttcacgtacgccatcatcgccgctggcgtggcccacgccatcaca
gctgcctgtacccaaggcaacctgagtgactgtggctgcgacaaggagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc
ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttacacaataacgaggcaggccgaaagatcctggaggaaaatatgaagctggagtgt
aagtgccatggtgtgtccggctcgtgcaccacaaagacatgctggacgacgctgccgcag
ttccgggagctgggctacgtgctcaaggacaagtacaacgaggcggtccatgtggagccc
gtgcgtgccagccgcaacaagcggcccaccttcctgaagatcaagaagccactgtcatac
cgcaagcccatggacacagacctggtgtacatcgagaagtcacccaactactgcgaggag
gacccggtgacgggcagtgtgggcacacagggccgcgcctgcaacaagacagccccgcag
gccagcggctgcgacctcatgtgctgtggccgcggctacaacacccaccagtatgcccgc
gtgtggcagtgcaactgcaagttccactggtgctgttacgtcaagtgcaacacctgcagc
gagcgcaccgaggtgtacacgtgcaagtga

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