KEGG   Ursus maritimus (polar bear): 103676602
Entry
103676602         CDS       T03271                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
umr  Ursus maritimus (polar bear)
Pathway
umr04150  mTOR signaling pathway
umr04310  Wnt signaling pathway
umr04390  Hippo signaling pathway
umr04550  Signaling pathways regulating pluripotency of stem cells
umr04916  Melanogenesis
umr04934  Cushing syndrome
umr05010  Alzheimer disease
umr05022  Pathways of neurodegeneration - multiple diseases
umr05165  Human papillomavirus infection
umr05200  Pathways in cancer
umr05202  Transcriptional misregulation in cancer
umr05205  Proteoglycans in cancer
umr05217  Basal cell carcinoma
umr05224  Breast cancer
umr05225  Hepatocellular carcinoma
umr05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:umr00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    103676602 (WNT16)
   04390 Hippo signaling pathway
    103676602 (WNT16)
   04150 mTOR signaling pathway
    103676602 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    103676602 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    103676602 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    103676602 (WNT16)
   05202 Transcriptional misregulation in cancer
    103676602 (WNT16)
   05205 Proteoglycans in cancer
    103676602 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    103676602 (WNT16)
   05226 Gastric cancer
    103676602 (WNT16)
   05217 Basal cell carcinoma
    103676602 (WNT16)
   05224 Breast cancer
    103676602 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    103676602 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    103676602 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    103676602 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    103676602 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:umr00536]
    103676602 (WNT16)
Glycosaminoglycan binding proteins [BR:umr00536]
 Heparan sulfate / Heparin
  Morphogens
   103676602 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 103676602
NCBI-ProteinID: XP_008704034
UniProt: A0A384DB61
LinkDB
Position
Unknown
AA seq 362 aa
MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLTSRQKELC
KRKPYLLPSIGEGARLGIQECRSQFRHERWNCLVTAASPPGTSPLFGYELSSGTKETAFI
YAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFL
DFPIKNTTGKESQVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFE
KIGHLLKDKYENSVQISDKIKRKMRRRDKDQRKIPIRKEDLLYVNKSPNYCVEDKKLGIP
GTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHT
CK
NT seq 1089 nt   +upstreamnt  +downstreamnt
atggacagagcggcgctcctgggactgtcgcgcctgtgcgcgctgtgggcagccctgctc
gcgctgttcccgtgcggagcccagggaaattggatgtggttgggcatcgcctcctttggg
gttccggagaagctgggctgcgccaacttgccgctgaccagccgccagaaggagctgtgc
aagaggaaaccgtacctgctgccgagcatcggagagggcgcgcggctgggcattcaggag
tgcaggagccagttcagacacgagagatggaactgcctggtcaccgccgcctccccgccg
ggcaccagccccctttttggctacgagctgagcagtggcaccaaggaaacagcatttatt
tatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcgtgcagtgcaggcaac
atgaccgagtgttcctgcgacaccaccttacagaatggcggctcggccagcgaaggctgg
cactgggggggctgctccgatgatgtccagtatggcatgtggttcagcagaaagttccta
gatttccccatcaaaaacacgacaggaaaagaaagccaagtactgttagcaatgaaccta
cacaacaacgaagctggaaggcaggccgtcgccaagctgatgtcggtagattgccgctgt
cacggagtttccggctcctgcgctgtgaaaacgtgctggaaaaccatgtcctctttcgaa
aagattggccatttgttgaaggataaatatgaaaacagtgtccaaatctcagacaaaata
aagaggaaaatgcgcaggagagacaaagatcagaggaaaataccgattcgcaaggaggat
ctgctctacgttaataagtctcccaattactgcgtagaggacaagaaactggggatcccg
ggcacgcaaggcagagaatgcaaccgcacgtcggagggcgcggacggctgcaacctcctc
tgctgtggccgaggctacaacacccacgtggtcaggcacgtggagaggtgcgagtgcaag
tttatttggtgctgctacgtgcgctgcagacggtgcgaaagcatgactgacgtccacact
tgcaagtag

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