KEGG   Ovis aries (sheep): 101103229
Entry
101103229         CDS       T03117                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
oas  Ovis aries (sheep)
Pathway
oas04150  mTOR signaling pathway
oas04310  Wnt signaling pathway
oas04390  Hippo signaling pathway
oas04550  Signaling pathways regulating pluripotency of stem cells
oas04916  Melanogenesis
oas04934  Cushing syndrome
oas05010  Alzheimer disease
oas05022  Pathways of neurodegeneration - multiple diseases
oas05165  Human papillomavirus infection
oas05200  Pathways in cancer
oas05202  Transcriptional misregulation in cancer
oas05205  Proteoglycans in cancer
oas05217  Basal cell carcinoma
oas05224  Breast cancer
oas05225  Hepatocellular carcinoma
oas05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:oas00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    101103229 (WNT16)
   04390 Hippo signaling pathway
    101103229 (WNT16)
   04150 mTOR signaling pathway
    101103229 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    101103229 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    101103229 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    101103229 (WNT16)
   05202 Transcriptional misregulation in cancer
    101103229 (WNT16)
   05205 Proteoglycans in cancer
    101103229 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    101103229 (WNT16)
   05226 Gastric cancer
    101103229 (WNT16)
   05217 Basal cell carcinoma
    101103229 (WNT16)
   05224 Breast cancer
    101103229 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    101103229 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101103229 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    101103229 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    101103229 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:oas00536]
    101103229 (WNT16)
Glycosaminoglycan binding proteins [BR:oas00536]
 Heparan sulfate / Heparin
  Morphogens
   101103229 (WNT16)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 101103229
NCBI-ProteinID: XP_004008061
EnsemblRapid: ENSOARG00020002230
LinkDB
Position
4:87462192..87473755
AA seq 362 aa
MDRAALLGLSRLCALWAAVLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KRKPYLLPSIREGARLGIQECRSQFRHERWNCLVAAASPPGTSPLFGYELSSGTKETAFI
YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMSFSRKFL
DFPIRNTTAKESKVLLAMNLHNNEAGRQAVAKLMSLDCRCHGVSGSCAVKTCWKTMSSFE
KIGHLLKDKYENSVQISDKIKKKMHRREKDQRKIPIRKDDLLYVNKSPNYCVEDKKLGIP
GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT
CK
NT seq 1089 nt   +upstreamnt  +downstreamnt
atggacagagcagcgctcctgggactgtcccgcctgtgcgcgctgtgggcagccgtgctc
gcgctgttcccctgcggagcccaaggaaactggatgtggttgggcatcgcctcctttggg
gttccagagaagctgggctgtgccaacttgcctctgaacagccgccagaaggagctgtgc
aagaggaaaccgtacctgctgccgagcattcgcgagggcgcccggctgggcattcaggag
tgcagaagccagttcaggcacgagagatggaactgcctggtggccgccgcctccccaccg
ggcaccagccctctctttggctacgagctgagcagcggcaccaaggaaacagcatttatt
tatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagcgcaggcaac
atgaccgagtgttcctgtgacaccaccttgcagaacggcggctcagcgagtgaaggctgg
cattgggggggatgctccgatgatgtccagtacggcatgtcattcagcagaaagttccta
gatttccccatcagaaacaccacggcaaaggaaagcaaagtactgttagcaatgaaccta
cataacaatgaagctggaaggcaggctgtcgccaagttgatgtccttagactgccgttgt
cacggagtttccggctcctgcgctgtaaaaacatgctggaaaaccatgtcttcttttgaa
aagattggccatctgttgaaggataaatatgaaaacagtgtccaaatctcagacaaaata
aagaagaaaatgcataggagagaaaaagatcagaggaaaataccaatccgcaaggatgat
ctgctctacgtcaataagtctcccaattactgtgttgaggataagaaactcgggatccca
gggactcaaggcagagagtgtaaccgcacgtcggagggcgcagatggctgcaacctcctc
tgctgtggccgaggctacaacacccatgtggtcaggcacgtggagagatgtgaatgcaaa
ttcatctggtgctgttatgtccgctgcaggaggtgcgaaagcatgactgatgtccacact
tgcaagtaa

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