KEGG   Mustela nigripes (black-footed ferret): 132014957
Entry
132014957         CDS       T09425                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
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
mnp05202  Transcriptional misregulation 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
    132014957 (WNT16)
   04390 Hippo signaling pathway
    132014957 (WNT16)
   04150 mTOR signaling pathway
    132014957 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    132014957 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    132014957 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    132014957 (WNT16)
   05202 Transcriptional misregulation in cancer
    132014957 (WNT16)
   05205 Proteoglycans in cancer
    132014957 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    132014957 (WNT16)
   05226 Gastric cancer
    132014957 (WNT16)
   05217 Basal cell carcinoma
    132014957 (WNT16)
   05224 Breast cancer
    132014957 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    132014957 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    132014957 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    132014957 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    132014957 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mnp00536]
    132014957 (WNT16)
Glycosaminoglycan binding proteins [BR:mnp00536]
 Heparan sulfate / Heparin
  Morphogens
   132014957 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 132014957
NCBI-ProteinID: XP_059251624
LinkDB
Position
4:complement(29024533..29034936)
AA seq 362 aa
MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KKKPYLLPSIGEGARLGIQECRSQFRHERWNCLVAAAAPPGTSPLFGYELSSGTKETAFI
YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL
DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE
KIGHLLKDKYENSVQISDKIKRKMRRRDKDQKKIPIRKDDLLYVNKSPNYCVEDKKLGIP
GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT
CK
NT seq 1089 nt   +upstreamnt  +downstreamnt
atggacagagcggcgctcctgggactgtcgcgcctgtgcgcgctgtgggcagccctgctc
gcgctgttcccctgcggagcccaaggaaattggatgtggttgggcatcgcctcctttggg
gttccggagaagctgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc
aagaagaaaccgtacctgctgccgagcatcggagagggcgcgcggctgggcattcaggag
tgcaggagccagttcagacacgagaggtggaactgcctggtcgccgccgccgccccgccg
ggcaccagccctctttttggctacgagctgagcagcggcaccaaggaaacagcatttatt
tatgctgtgatggcagcaggcctggtgcattctgtgaccaggtcttgcagtgcaggcaac
atgaccgagtgctcctgtgacaccaccttacagaacggcggttcagcaagcgaaggctgg
cactgggggggctgctccgatgatgtccagtatggcatgtggttcagcagaaagttccta
gatttccccatcagaaacactacaggaaaagaaagcaaagtacttttagcaatgaacctg
cacaacaacgaagctggaaggcaggctgtcgccaagttgatgtccgtggattgccgatgt
cacggagtttccggctcctgcgctgtgaaaacgtgctggaaaactatgtcttcttttgaa
aagattggccacttgttgaaggataagtacgaaaacagtgtccaaatctcggacaaaata
aagaggaaaatgcgcagaagagacaaagatcagaagaaaatacccattcgcaaggatgat
ctcctctacgttaataagtctcccaattactgtgtcgaggataagaaactagggatcccc
gggacccaaggcagagaatgcaaccgcacgtcggagggcgcggacggctgcaacctcctc
tgctgtggccgaggctacaacacccacgtggtcaggcacgtggagaggtgcgagtgcaag
tttatttggtgctgctacgtccgctgcaggaggtgtgaaagcatgactgacgtccacact
tgcaagtag

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