KEGG   Echinops telfairi (small Madagascar hedgehog): 101653677
Entry
101653677         CDS       T08707                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
etf  Echinops telfairi (small Madagascar hedgehog)
Pathway
etf04150  mTOR signaling pathway
etf04310  Wnt signaling pathway
etf04390  Hippo signaling pathway
etf04550  Signaling pathways regulating pluripotency of stem cells
etf04916  Melanogenesis
etf04934  Cushing syndrome
etf05010  Alzheimer disease
etf05022  Pathways of neurodegeneration - multiple diseases
etf05165  Human papillomavirus infection
etf05200  Pathways in cancer
etf05202  Transcriptional misregulation in cancer
etf05205  Proteoglycans in cancer
etf05217  Basal cell carcinoma
etf05224  Breast cancer
etf05225  Hepatocellular carcinoma
etf05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:etf00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101653677 (WNT16)
   04390 Hippo signaling pathway
    101653677 (WNT16)
   04150 mTOR signaling pathway
    101653677 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101653677 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101653677 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101653677 (WNT16)
   05202 Transcriptional misregulation in cancer
    101653677 (WNT16)
   05205 Proteoglycans in cancer
    101653677 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101653677 (WNT16)
   05226 Gastric cancer
    101653677 (WNT16)
   05217 Basal cell carcinoma
    101653677 (WNT16)
   05224 Breast cancer
    101653677 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101653677 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101653677 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    101653677 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101653677 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:etf00536]
    101653677 (WNT16)
Glycosaminoglycan binding proteins [BR:etf00536]
 Heparan sulfate / Heparin
  Morphogens
   101653677 (WNT16)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 101653677
NCBI-ProteinID: XP_004707830
LinkDB
Position
Unknown
AA seq 361 aa
MNRVALLGLPRLCALWAALFTLFPCGAQGNWMWLGIASFGVPEKLGCANLPLSSRQKELC
KRKPYLLPSIREGARLGIQECRSQFRHERWNCAVAAAPAATSPVFGYELSSGTKETAFIH
AVMAAGLVHSVTRSCSAGNMTECSCDTSLQNGGSASEGWHWGGCSDDVQYGMWFSRKFLD
FPIGNTTDKESKVLLAMNQHNNEAGRQAVAKLMSVDCRCHGVSGSCAVRTCWKTMPSFEK
IGHLLKDKYENSIQISDKITRKMRRREKAERKTPIRQDDLLYMNKSPNYCVEDKKLGIPG
TQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHTC
K
NT seq 1086 nt   +upstreamnt  +downstreamnt
atgaacagagtggcactcctgggcctgccccgcctgtgcgcgctgtgggcagccctgttc
acgctcttcccctgcggagcccaaggaaactggatgtggctgggcatcgcctcctttggg
gtgcccgagaagctgggctgcgccaacttgccgctgagcagccgccagaaggagctgtgc
aagcggaagccgtacctgctgcccagcatccgcgagggtgcgcgcctgggcatccaggag
tgccgcagccagttccggcacgagcgatggaactgcgcggtggcggccgcgcccgccgcc
accagcccggtcttcggctacgagctgagcagcggcacgaaggaaacagcgttcattcat
gcagtgatggctgccggcctggtgcactcggtgaccaggtcttgcagtgcaggcaacatg
acagagtgctcctgtgacaccagcctgcagaacgggggctcggcgagcgaaggctggcac
tgggggggctgctctgacgatgtccagtacggcatgtggttcagcagaaagttcctcgat
ttccccatcggaaacaccacggacaaagaaagcaaagttctcctagcaatgaaccagcat
aacaatgaagcgggaaggcaggccgtcgccaagttgatgtccgtggactgccgctgccac
ggggtttcaggatcctgtgctgtgaggacatgctggaaaaccatgccctccttcgagaag
atcggtcatttgttaaaggacaaatacgagaacagtatccaaatctcggacaaaatcacg
aggaaaatgcgcaggcgagagaaagcggagaggaaaacgccgatccgccaggacgatctg
ctatacatgaataagtcccccaactactgcgtggaggacaagaaactggggatccccggc
acgcaaggcagggagtgtaaccgcacttcggagggcgccgacgggtgcaacctgctgtgc
tgtggccggggctacaacacccacgtggtccggcacgtggagaggtgcgagtgtaagttc
atctggtgctgctacgtccgctgccgccgatgcgaaagcatgaccgacgtgcacacctgc
aagtga

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