KEGG   Myotis daubentonii (Daubenton's bat): 132242692
Entry
132242692         CDS       T10294                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
mdt  Myotis daubentonii (Daubenton's bat)
Pathway
mdt04150  mTOR signaling pathway
mdt04310  Wnt signaling pathway
mdt04390  Hippo signaling pathway
mdt04550  Signaling pathways regulating pluripotency of stem cells
mdt04916  Melanogenesis
mdt04934  Cushing syndrome
mdt05010  Alzheimer disease
mdt05022  Pathways of neurodegeneration - multiple diseases
mdt05165  Human papillomavirus infection
mdt05200  Pathways in cancer
mdt05202  Transcriptional misregulation in cancer
mdt05205  Proteoglycans in cancer
mdt05217  Basal cell carcinoma
mdt05224  Breast cancer
mdt05225  Hepatocellular carcinoma
mdt05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mdt00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    132242692 (WNT16)
   04390 Hippo signaling pathway
    132242692 (WNT16)
   04150 mTOR signaling pathway
    132242692 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    132242692 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    132242692 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    132242692 (WNT16)
   05202 Transcriptional misregulation in cancer
    132242692 (WNT16)
   05205 Proteoglycans in cancer
    132242692 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    132242692 (WNT16)
   05226 Gastric cancer
    132242692 (WNT16)
   05217 Basal cell carcinoma
    132242692 (WNT16)
   05224 Breast cancer
    132242692 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    132242692 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    132242692 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    132242692 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    132242692 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mdt00536]
    132242692 (WNT16)
Glycosaminoglycan binding proteins [BR:mdt00536]
 Heparan sulfate / Heparin
  Morphogens
   132242692 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 132242692
NCBI-ProteinID: XP_059567643
LinkDB
Position
10:16771211..16781494
AA seq 361 aa
MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KRKPYLLPSIREGARLGVQECRSQFRHERWDCRVAAAPSAASPLFGYELSSGTKETAFIY
AVMAAGLVHAVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFLD
FPIRNTTGRESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFEK
IGHFLKDKYEHSVQVSDKIKRKMRRREKDQRKVPIRKEDLLYIHKSPNYCVEDKKIGIPG
TQGRECNRTSEGAGGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHTC
K
NT seq 1086 nt   +upstreamnt  +downstreamnt
atggaccgagcggcgctcctgggactgtcccgcctgtgcgcgctgtgggcagccctgctc
gcgctgttcccctgcggggcccaaggaaactggatgtggttgggcatcgcctccttcggg
gtcccggagaagctgggctgcgccaacttgccgctgaacagccggcagaaggagctgtgc
aagaggaagccctacctgctgcccagcatccgcgagggcgcgcgcctgggcgtccaggag
tgccgcagccagttccgccacgagcgctgggactgccgcgtggccgccgccccctcggcc
gccagccccctcttcggctacgagctgagcagcggcaccaaggaaacagcgtttatctac
gcggtgatggctgcaggcctggtgcacgcggtgaccaggtcatgcagcgcaggcaacatg
acggagtgttcctgtgacaccaccttgcagaacggcggctcagccagcgaaggctggcac
tgggggggctgctcggatgacgtccagtacggcatgtggttcagcagaaagttcctggac
ttccccatcagaaacaccacgggcagagaaagcaaagtgctgttagcgatgaaccttcat
aacaatgaagctggaaggcaggctgtggccaagctgatgtccgtggactgccgctgtcac
ggcgtgtccggctcctgtgcggtgaaaacatgctggaaaaccatgtcttcttttgagaag
attggccatttcctgaaggataaatatgagcacagtgttcaagtctcagacaaaataaaa
aggaaaatgcgcaggagagaaaaggaccagaggaaagtaccgatccgcaaggaggatctg
ctctacatccataagtctcccaactactgtgtagaggataagaaaattgggatcccgggg
acacagggccgagaatgcaaccgcacgtcggagggcgcgggtggctgcaacctcctctgc
tgtggccgaggctacaacacccacgtggtcagacacgtggagaggtgcgagtgcaagttc
atctggtgctgctacgttcgctgcaggaggtgtgaaagcatgactgacgtccacacctgc
aagtaa

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