KEGG   Rousettus aegyptiacus (Egyptian rousette): 107500238
Entry
107500238         CDS       T06036                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
ray  Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04150  mTOR signaling pathway
ray04310  Wnt signaling pathway
ray04390  Hippo signaling pathway
ray04550  Signaling pathways regulating pluripotency of stem cells
ray04916  Melanogenesis
ray04934  Cushing syndrome
ray05010  Alzheimer disease
ray05022  Pathways of neurodegeneration - multiple diseases
ray05165  Human papillomavirus infection
ray05200  Pathways in cancer
ray05202  Transcriptional misregulation in cancer
ray05205  Proteoglycans in cancer
ray05217  Basal cell carcinoma
ray05224  Breast cancer
ray05225  Hepatocellular carcinoma
ray05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:ray00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    107500238 (WNT16)
   04390 Hippo signaling pathway
    107500238 (WNT16)
   04150 mTOR signaling pathway
    107500238 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    107500238 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    107500238 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    107500238 (WNT16)
   05202 Transcriptional misregulation in cancer
    107500238 (WNT16)
   05205 Proteoglycans in cancer
    107500238 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    107500238 (WNT16)
   05226 Gastric cancer
    107500238 (WNT16)
   05217 Basal cell carcinoma
    107500238 (WNT16)
   05224 Breast cancer
    107500238 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    107500238 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    107500238 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    107500238 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    107500238 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:ray00536]
    107500238 (WNT16)
Glycosaminoglycan binding proteins [BR:ray00536]
 Heparan sulfate / Heparin
  Morphogens
   107500238 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 107500238
NCBI-ProteinID: XP_015980743
UniProt: A0A7J8D961
LinkDB
Position
Unknown
AA seq 362 aa
MDRVALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KRKPYLLPSIREGARLGIQECRSQFRHERWNCQVSTAAPPGTSPLFGYELSSGTKETAFI
YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL
DFPTRNTTGKENKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE
KIGHLLKDKYENSVQVSDRIKRKMRRREKDQKKELIRKDDLLYINKSPNYCVEDKKLGIP
GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT
CK
NT seq 1089 nt   +upstreamnt  +downstreamnt
atggacagagtggcgctcctgggactgtcacgcctgtgcgcgctgtgggcagccctgctc
gcactgttcccctgcggagcccaaggaaactggatgtggttgggcatcgcctcctttggg
gttccggagaaactgggctgcgccaacttgccgctgaacagccggcagaaggagctgtgc
aagaggaaaccgtacctgctgcccagcatccgagagggcgcccggctgggcattcaggag
tgcaggagccagtttagacacgagagatggaactgccaggtctctaccgccgccccaccg
ggcaccagtcccctctttggctacgagctgagcagcggcaccaaggaaacagcatttatt
tatgccgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagtgcaggcaac
atgacggagtgttcctgtgacaccactttgcagaatggtggctcagcaagtgaaggctgg
cattgggggggctgctccgatgatgttcagtatggcatgtggttcagcagaaagttccta
gatttccccaccagaaacaccacgggaaaagaaaacaaagtactgttagcaatgaatcta
cataacaatgaagctggaaggcaggctgtcgccaagttgatgtcagtggactgccgctgc
cacggagtttccggctcctgtgctgtgaaaacgtgctggaaaaccatgtcttcttttgaa
aaaattggccatttgttgaaggataaatatgaaaacagtgttcaagtctcagacagaata
aagaggaaaatgcgcagaagagaaaaagaccagaagaaagaattaatccgcaaggatgat
ctgctttacattaataagtctcccaattactgtgtagaggataagaaattagggatccct
ggtacacaaggcagagaatgcaaccgtacatccgagggcgcggatggatgcaacctcctc
tgctgtggccgaggctataacacccacgtggtcaggcacgtggagaggtgtgagtgcaag
tttatctggtgctgctatgttcgctgcaggaggtgtgaaagcatgacggatgtccacact
tgcaaataa

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