KEGG   Equus caballus (horse): 100071393
Entry
100071393         CDS       T01058                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
ecb  Equus caballus (horse)
Pathway
ecb04150  mTOR signaling pathway
ecb04310  Wnt signaling pathway
ecb04390  Hippo signaling pathway
ecb04550  Signaling pathways regulating pluripotency of stem cells
ecb04916  Melanogenesis
ecb04934  Cushing syndrome
ecb05010  Alzheimer disease
ecb05022  Pathways of neurodegeneration - multiple diseases
ecb05165  Human papillomavirus infection
ecb05200  Pathways in cancer
ecb05202  Transcriptional misregulation in cancer
ecb05205  Proteoglycans in cancer
ecb05217  Basal cell carcinoma
ecb05224  Breast cancer
ecb05225  Hepatocellular carcinoma
ecb05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ecb00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    100071393 (WNT16)
   04390 Hippo signaling pathway
    100071393 (WNT16)
   04150 mTOR signaling pathway
    100071393 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    100071393 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    100071393 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    100071393 (WNT16)
   05202 Transcriptional misregulation in cancer
    100071393 (WNT16)
   05205 Proteoglycans in cancer
    100071393 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    100071393 (WNT16)
   05226 Gastric cancer
    100071393 (WNT16)
   05217 Basal cell carcinoma
    100071393 (WNT16)
   05224 Breast cancer
    100071393 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    100071393 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100071393 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    100071393 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    100071393 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ecb00536]
    100071393 (WNT16)
Glycosaminoglycan binding proteins [BR:ecb00536]
 Heparan sulfate / Heparin
  Morphogens
   100071393 (WNT16)
SSDB
Motif
Pfam: wnt
Other DBs
NCBI-GeneID: 100071393
NCBI-ProteinID: XP_001917264
LinkDB
Position
4:77823771..77835685
AA seq 405 aa
MLSAGGKKARDNLVLGTDLWPGGLLGGESRRGVTGAGGLHAGAMDRAALLGLSRLCALWA
ALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELCKRKPYLLPSIREGARLG
IQECRNQFRHERWNCRVAATAPPGTSPIFGYELTSGTKETAFIYAVMAAGLVHSVTRSCS
AGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFLDVPNKNTTGKESKILLA
MNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFEKIGHLLKDKYENSVQIS
DKIKRKMRRREKDQRKIPIHKEDLFYINKSPNYCVEDKKLGIPGTQGRECNRTSEGADGC
NLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHTCK
NT seq 1218 nt   +upstreamnt  +downstreamnt
atgttgtctgcagggggaaagaaggcgagggacaacttggtgctgggaactgacctctgg
cctggcgggcttctgggaggggagagcagaagaggagtgactggggctgggggactccat
gcgggggccatggacagagcggcgctcctgggactgtcccgcctttgcgcgctgtgggca
gccctgctcgcgctgttcccatgcggagcccaaggaaactggatgtggttgggcatcgcc
tcctttggggttccggagaagctgggctgcgccaacttgccgctgaacagccgccagaag
gagctgtgcaagaggaaaccgtacctgctgccgagcatccgagagggcgcccggctgggc
attcaggagtgcaggaaccagttcagacacgagaggtggaactgccgggttgccgccacc
gccccgccgggcaccagccccatctttggctacgagctgaccagcggcaccaaggaaaca
gcatttatttatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagt
gcaggcaacatgacggagtgttcctgtgataccaccttgcagaatggcggctcagccagt
gaaggctggcactgggggggctgctctgatgatgtgcaatatggcatgtggttcagcaga
aagttcctagatgtccccaacaaaaacaccacgggaaaagaaagcaaaatactgttagca
atgaacctacataacaatgaagctggaaggcaggctgtcgccaagttgatgtcagtagac
tgccgctgccacggagtttccggttcctgtgctgtgaaaacatgctggaaaaccatgtct
tcttttgaaaagattggccatttgttgaaggataaatatgaaaacagtgtgcaaatctca
gacaaaataaagaggaaaatgcgcaggagagaaaaagatcagaggaaaatacccatccac
aaggaggatctgttctacattaataagtctcccaattactgtgtagaggataagaaacta
gggatcccagggacacaaggcagagaatgcaaccgtacgtcggagggtgcagatggctgc
aacctcctctgctgtggccgaggctacaacacccacgtggtcaggcatgtggagaggtgt
gagtgcaagtttatctggtgctgctatgtccgctgcaggaggtgtgaaagcatgactgac
gtccacacttgcaagtaa

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