KEGG   Mirounga leonina (Southern elephant seal): 118021382
Entry
118021382         CDS       T07472                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16 isoform X1
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
mlx  Mirounga leonina (Southern elephant seal)
Pathway
mlx04150  mTOR signaling pathway
mlx04310  Wnt signaling pathway
mlx04390  Hippo signaling pathway
mlx04550  Signaling pathways regulating pluripotency of stem cells
mlx04916  Melanogenesis
mlx04934  Cushing syndrome
mlx05010  Alzheimer disease
mlx05022  Pathways of neurodegeneration - multiple diseases
mlx05165  Human papillomavirus infection
mlx05200  Pathways in cancer
mlx05202  Transcriptional misregulation in cancer
mlx05205  Proteoglycans in cancer
mlx05217  Basal cell carcinoma
mlx05224  Breast cancer
mlx05225  Hepatocellular carcinoma
mlx05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:mlx00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    118021382 (WNT16)
   04390 Hippo signaling pathway
    118021382 (WNT16)
   04150 mTOR signaling pathway
    118021382 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    118021382 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    118021382 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    118021382 (WNT16)
   05202 Transcriptional misregulation in cancer
    118021382 (WNT16)
   05205 Proteoglycans in cancer
    118021382 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    118021382 (WNT16)
   05226 Gastric cancer
    118021382 (WNT16)
   05217 Basal cell carcinoma
    118021382 (WNT16)
   05224 Breast cancer
    118021382 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    118021382 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    118021382 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    118021382 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    118021382 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:mlx00536]
    118021382 (WNT16)
Glycosaminoglycan binding proteins [BR:mlx00536]
 Heparan sulfate / Heparin
  Morphogens
   118021382 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 118021382
NCBI-ProteinID: XP_034877342
LinkDB
Position
Unknown
AA seq 391 aa
MRAAGAHGGCGKRGAQPQGTFSWSRGAGPGILGRMTQFSAKPLGLERRAGERLTLGAAVS
YRWLGIASFGVPEKLGCANLPLNSRQKELCKRKPYLLPSIGEGARLGIQECRSQFRHERW
NCLVTAAPPGTSPLFGYELSSGTKETAFIYAVMAAGLVHSVTRSCSAGNMTECSCDTSLQ
SGGSASEGWHWGGCSDDVQYGMWFSRKFLDLPVRNSTGKESKVLLAMNLHNNEAGRQAVA
KLMSVDCRCHGVSGSCAVKTCWKTMSSFEKIGHLLKDKYENSVQISDKIKRKMRRRDKDQ
RKIPIRKDDLLYVNKSPNYCVEDKKLGIPGTQGRECNRTSEGADGCNLLCCGRGYNTHVV
RHVERCECKFIWCCYVRCRRCESMTDVHTCK
NT seq 1176 nt   +upstreamnt  +downstreamnt
atgcgggcagcaggggcgcacgggggttgcggcaaaaggggtgcccagcctcagggcact
ttcagctggagccggggagcaggaccggggatcctagggcggatgacccaattttcggcg
aaacctctgggattggagaggagagctggggagcggctcacgctaggggcggcggtgtct
tacaggtggttgggcatcgcgtcctttggggttccggagaagctgggctgcgccaacttg
ccgctgaacagccgccagaaggagctgtgcaagaggaaaccgtacctgctgccgagcatc
ggagagggcgcgcggctgggcattcaggagtgccggagccagttccggcacgagaggtgg
aactgcctggtcaccgccgccccgccgggcaccagccccctttttggctacgagctgagc
agcggcaccaaggaaacagcatttatttatgctgtgatggctgcaggcctggtgcattct
gtgaccaggtcctgcagtgcaggcaacatgaccgagtgctcctgcgacaccagcttgcag
agcggcggctccgccagtgaaggctggcactgggggggctgctcggatgatgtccagtat
ggcatgtggttcagcaggaagttcctagatctccccgtcagaaacagcacaggaaaagaa
agcaaagtactgttagcaatgaatctacacaacaacgaagccggaaggcaggctgtcgcc
aagttgatgtccgtagattgccgctgtcacggagtttcgggctcctgcgctgtgaaaacg
tgctggaaaaccatgtcttctttcgagaagattggccacttgctgaaggataaatacgaa
aacagtgtccaaatctcagacaaaataaagaggaaaatgcgcaggagagacaaggatcag
aggaaaataccgattcgcaaggatgatctgctctacgtcaataagtctcccaattactgt
gtcgaggataagaaactagggatcccggggacacaaggcagagaatgcaaccgcacgtca
gagggcgcggacggctgcaacctcctttgctgtggccgaggctacaacacccacgtggtc
aggcacgtggagaggtgcgagtgcaagtttatttggtgctgctacgttcgctgcaggagg
tgtgaaagcatgactgacgtccacacttgcaagtag

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