KEGG   Mustela lutreola (European mink): 131829677
Entry
131829677         CDS       T09578                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
mlk  Mustela lutreola (European mink)
Pathway
mlk04150  mTOR signaling pathway
mlk04310  Wnt signaling pathway
mlk04390  Hippo signaling pathway
mlk04550  Signaling pathways regulating pluripotency of stem cells
mlk04916  Melanogenesis
mlk04934  Cushing syndrome
mlk05010  Alzheimer disease
mlk05022  Pathways of neurodegeneration - multiple diseases
mlk05165  Human papillomavirus infection
mlk05200  Pathways in cancer
mlk05202  Transcriptional misregulation in cancer
mlk05205  Proteoglycans in cancer
mlk05217  Basal cell carcinoma
mlk05224  Breast cancer
mlk05225  Hepatocellular carcinoma
mlk05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mlk00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    131829677 (WNT16)
   04390 Hippo signaling pathway
    131829677 (WNT16)
   04150 mTOR signaling pathway
    131829677 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    131829677 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    131829677 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    131829677 (WNT16)
   05202 Transcriptional misregulation in cancer
    131829677 (WNT16)
   05205 Proteoglycans in cancer
    131829677 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    131829677 (WNT16)
   05226 Gastric cancer
    131829677 (WNT16)
   05217 Basal cell carcinoma
    131829677 (WNT16)
   05224 Breast cancer
    131829677 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    131829677 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    131829677 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    131829677 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    131829677 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mlk00536]
    131829677 (WNT16)
Glycosaminoglycan binding proteins [BR:mlk00536]
 Heparan sulfate / Heparin
  Morphogens
   131829677 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 131829677
NCBI-ProteinID: XP_059027670
LinkDB
Position
4:173394199..173406129
AA seq 362 aa
MDRAALLGLSRLCALWVALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KKKPYLLPSIGEGARLGIQECRSQFRHERWNCLVTAAAPPGTSPLFGYELSSGTKETAFI
YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL
DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE
KIGHLLKDKYENSVQISDKIKRKMRRRDKDQRKIPIRKDDLLYVNKSPNYCVEDKKLGIP
GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT
CK
NT seq 1089 nt   +upstreamnt  +downstreamnt
atggacagagcggcgctcctgggactgtcgcgcctgtgcgcgctgtgggtagccctgctc
gcgctgttcccctgcggagcccaaggaaattggatgtggttgggcatcgcctcctttggg
gttccggagaagctgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc
aagaagaaaccgtacctgctgccgagcatcggagagggcgcgcggctgggcattcaggag
tgcaggagccagttcagacacgagaggtggaactgcctggtcaccgccgccgccccgccg
ggcaccagccctctttttggctacgagctgagcagcggcaccaaggaaacagcatttatt
tatgctgtgatggcagcaggcctggtgcattctgtgaccaggtcttgcagtgcaggcaac
atgaccgagtgctcctgtgacaccaccttacagaacggcggttcagcaagcgaaggctgg
cactgggggggctgctccgatgatgtccagtatggcatgtggttcagcagaaagttccta
gatttccccatcagaaacactacaggaaaagaaagcaaagtacttttagcaatgaacctg
cacaacaacgaagctggaaggcaggctgtcgccaagttgatgtccgtggattgccgatgt
cacggagtttccggctcctgcgctgtgaaaacgtgctggaaaactatgtcttcttttgaa
aagattggccacctgttgaaggataagtacgaaaacagtgtccaaatctcggacaaaata
aagaggaaaatgcgcagaagagacaaagatcagaggaaaatacccattcgcaaggatgat
ctcctctacgttaataagtctcccaattactgtgtcgaggataagaaactagggatcccc
gggacccaaggcagagaatgcaaccgcacgtcggagggcgcggacggctgcaacctcctc
tgctgtggccgaggctacaacacccacgtggtcaggcacgtggagaggtgcgagtgcaag
tttatttggtgctgctacgtccgctgcaggaggtgtgaaagcatgactgacgtccacact
tgcaagtag

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