KEGG   Desmodus rotundus (common vampire bat): 112299924
Entry
112299924         CDS       T05907                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
dro  Desmodus rotundus (common vampire bat)
Pathway
dro04150  mTOR signaling pathway
dro04310  Wnt signaling pathway
dro04390  Hippo signaling pathway
dro04550  Signaling pathways regulating pluripotency of stem cells
dro04916  Melanogenesis
dro04934  Cushing syndrome
dro05010  Alzheimer disease
dro05022  Pathways of neurodegeneration - multiple diseases
dro05165  Human papillomavirus infection
dro05200  Pathways in cancer
dro05202  Transcriptional misregulation in cancer
dro05205  Proteoglycans in cancer
dro05217  Basal cell carcinoma
dro05224  Breast cancer
dro05225  Hepatocellular carcinoma
dro05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:dro00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    112299924 (WNT16)
   04390 Hippo signaling pathway
    112299924 (WNT16)
   04150 mTOR signaling pathway
    112299924 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    112299924 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    112299924 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    112299924 (WNT16)
   05202 Transcriptional misregulation in cancer
    112299924 (WNT16)
   05205 Proteoglycans in cancer
    112299924 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    112299924 (WNT16)
   05226 Gastric cancer
    112299924 (WNT16)
   05217 Basal cell carcinoma
    112299924 (WNT16)
   05224 Breast cancer
    112299924 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    112299924 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    112299924 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    112299924 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    112299924 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:dro00536]
    112299924 (WNT16)
Glycosaminoglycan binding proteins [BR:dro00536]
 Heparan sulfate / Heparin
  Morphogens
   112299924 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 112299924
NCBI-ProteinID: XP_024410927
LinkDB
Position
Unknown
AA seq 362 aa
MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KRKPYLLPSIREGARLGIQECRSQFRHERWNCQVAAAAPPGTSPLFGYELSSGTKETAFI
YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL
DFPIRNTTGKESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE
KIGHLLKDKYENSIQVSDKLKRKMRRRDKDQRKVPIHKDDLLYVNKSPNYCVEDKKLGIP
GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT
CK
NT seq 1089 nt   +upstreamnt  +downstreamnt
atggacagagcggcgctcctgggactgtcccgcttgtgcgcgctttgggcagccctgctc
gcgctgttcccttgcggagcccaaggaaactggatgtggttgggcatcgcctcctttggg
gttccggagaaactgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc
aagaggaaaccgtacctgctgcccagcatccgagagggcgcccggctgggcattcaggag
tgcaggagccagttcagacacgagagatggaactgccaggtggccgccgccgccccgccg
ggcaccagccccctctttggctacgagctgagcagcggcaccaaggaaacggcgttcatt
tacgccgtgatggccgcgggcctggtgcattccgtgaccaggtcgtgcagtgcaggcaac
atgacggagtgctcctgtgacaccaccttgcagaacggtggctcagcgagtgaaggctgg
cactggggaggctgctccgatgatgtccagtatggcatgtggttcagccgaaagttccta
gatttccccatcagaaacaccacgggaaaagaaagcaaagtactgttagcaatgaacctt
cataacaatgaagctggaaggcaggctgtggctaagctgatgtcagtagactgccgctgt
catggagtttccggctcctgtgctgtaaaaacatgctggaaaaccatgtcttcttttgaa
aagattggacatttgttgaaagataaatatgaaaacagcattcaagtctcagacaaacta
aagaggaaaatgcgcaggagagacaaagaccagaggaaagtaccgatccacaaggatgac
ctgctctacgttaacaagtctcccaactactgtgtggaggataagaaattagggatccca
gggacacaaggcagagaatgcaaccgtacgtccgagggtgcggacggctgcaacctcctc
tgctgcggccgaggctacaacacccacgtggtcagacacgtggagaggtgtgagtgcaag
ttcatctggtgctgctatgttcgctgcaggaggtgtgaaagcatgactgatgtccacact
tgcaagtaa

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