KEGG   Mustela nigripes (black-footed ferret): 132027458
Entry
132027458         CDS       T09425                                 
Symbol
WNT3A
Name
(RefSeq) protein Wnt-3a
  KO
K00312  wingless-type MMTV integration site family, member 3
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
mnp05206  MicroRNAs 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
    132027458 (WNT3A)
   04390 Hippo signaling pathway
    132027458 (WNT3A)
   04150 mTOR signaling pathway
    132027458 (WNT3A)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    132027458 (WNT3A)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    132027458 (WNT3A)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    132027458 (WNT3A)
   05206 MicroRNAs in cancer
    132027458 (WNT3A)
   05205 Proteoglycans in cancer
    132027458 (WNT3A)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    132027458 (WNT3A)
   05226 Gastric cancer
    132027458 (WNT3A)
   05217 Basal cell carcinoma
    132027458 (WNT3A)
   05224 Breast cancer
    132027458 (WNT3A)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    132027458 (WNT3A)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    132027458 (WNT3A)
   05022 Pathways of neurodegeneration - multiple diseases
    132027458 (WNT3A)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    132027458 (WNT3A)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mnp00536]
    132027458 (WNT3A)
Glycosaminoglycan binding proteins [BR:mnp00536]
 Heparan sulfate / Heparin
  Morphogens
   132027458 (WNT3A)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 132027458
NCBI-ProteinID: XP_059272267
LinkDB
Position
12:156213994..156254868
AA seq 352 aa
MALLGYFLFLYGLEQALGSYPIWWSLAIGPQYSSLGTQPILCASIPGLVPKQLRFCRNYV
EIMPSVAEGVKISIQECQHQFRGRRWNCTTVDNSLAIFGPVLDRATRESAFVHAIASAGV
AFAVTRSCAEGSAAICGCSSRHQGLPGEGWKWGGCSEDIEFGGMVSREFADARENRPDAR
SAMNRHNNEAGRQAIASHMHLKCKCHGLSGSCEVKTCWWSQPDFRAIGDFLKDKYDSASE
MVVEKHRESRGWVETLRPRYTYFKVPTERDLVYYEASPNFCEPNPETGSFGTRDRTCNVS
SHGIDGCDLLCCGRGHNARTERRREKCHCVFHWCCYVSCQECARVYDVHTCK
NT seq 1059 nt   +upstreamnt  +downstreamnt
atggccctgctcggatacttcttattcctctacggcctggagcaggcgctgggcagctac
ccgatctggtggtcactggccatcgggccacagtattcgtccctgggcactcagcccatc
ctgtgtgccagcatccctggcctggtccccaagcagctgcgcttctgccggaactatgtg
gagatcatgcccagtgtggcggagggcgtgaagatcagcatccaggagtgtcagcaccag
ttccgcggccgccgctggaattgtaccactgtggacaacagcctggccatctttggccct
gtgctggacagagccacgcgggaatctgcctttgtgcacgccatcgcctctgccggcgtg
gccttcgctgtgacgcgctcatgcgctgagggctcggcggccatctgtggctgcagcagc
cggcaccagggcttgccgggcgagggctggaagtggggcggctgcagtgaggacatcgaa
tttggcggcatggtgtctcgggagtttgccgatgcgcgggagaaccggccagacgcccgc
tccgcgatgaaccgtcacaacaacgaggctggccgccaggccatcgccagccacatgcat
ctcaagtgcaagtgccacgggctgtcgggcagctgtgaggtgaagacctgctggtggtcg
cagcccgacttccgtgccatcggcgacttcctcaaggacaagtacgacagcgcctcggag
atggtcgtggagaagcaccgcgagtcgcgcggctgggtggaaaccctgcggccgcgctac
acctacttcaaggtgcccacggagcgcgatctggtgtactacgaggcctcgcccaacttc
tgcgaacccaaccccgagaccggctcgtttggcacgcgcgaccgcacgtgcaacgtgagc
tcgcatggcatcgatggctgcgacctgctgtgctgcggccgaggccacaacgcgcgcacc
gaacggcgccgcgagaagtgccactgcgtcttccactggtgctgctacgtgagctgccag
gagtgcgcgcgcgtctacgacgtgcacacatgcaagtag

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