KEGG   Myotis yumanensis (Yuma myotis): 139016796
Entry
139016796         CDS       T10762                                 
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
  KO
K01558  wingless-type MMTV integration site family, member 16
Organism
myum  Myotis yumanensis (Yuma myotis)
Pathway
myum04150  mTOR signaling pathway
myum04310  Wnt signaling pathway
myum04390  Hippo signaling pathway
myum04550  Signaling pathways regulating pluripotency of stem cells
myum04916  Melanogenesis
myum04934  Cushing syndrome
myum05010  Alzheimer disease
myum05022  Pathways of neurodegeneration - multiple diseases
myum05165  Human papillomavirus infection
myum05200  Pathways in cancer
myum05202  Transcriptional misregulation in cancer
myum05205  Proteoglycans in cancer
myum05217  Basal cell carcinoma
myum05224  Breast cancer
myum05225  Hepatocellular carcinoma
myum05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:myum00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    139016796 (WNT16)
   04390 Hippo signaling pathway
    139016796 (WNT16)
   04150 mTOR signaling pathway
    139016796 (WNT16)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    139016796 (WNT16)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    139016796 (WNT16)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    139016796 (WNT16)
   05202 Transcriptional misregulation in cancer
    139016796 (WNT16)
   05205 Proteoglycans in cancer
    139016796 (WNT16)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    139016796 (WNT16)
   05226 Gastric cancer
    139016796 (WNT16)
   05217 Basal cell carcinoma
    139016796 (WNT16)
   05224 Breast cancer
    139016796 (WNT16)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    139016796 (WNT16)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    139016796 (WNT16)
   05022 Pathways of neurodegeneration - multiple diseases
    139016796 (WNT16)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    139016796 (WNT16)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:myum00536]
    139016796 (WNT16)
Glycosaminoglycan binding proteins [BR:myum00536]
 Heparan sulfate / Heparin
  Morphogens
   139016796 (WNT16)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 139016796
NCBI-ProteinID: XP_070281105
LinkDB
Position
Unknown
AA seq 361 aa
MDRAALLGLSRLCALWAALLALFPCGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KRKPYLLPSIREGARLGVQECRSQFRHERWDCRVAAAPSAASPLFGYELSSGTKETAFIY
AVMAAGLVHAVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSRKFLD
FPIRNTTGRESKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMSSFEK
IGHFLKDKYEHSVQVSDKIKRKMRRREKDQRKVPIRKEDLLYIHKSPNYCVEDKKIGIPG
TQGRECNRTSEGAGGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTDVHTC
K
NT seq 1086 nt   +upstreamnt  +downstreamnt
atggaccgagcggcgctcctgggactgtcccgcctgtgcgcgctgtgggcagccctgctc
gcgctgttcccctgcggggcccaaggaaactggatgtggttgggcatcgcctccttcggg
gtcccggagaagctgggctgcgccaacttgccgctgaacagccgccagaaggagctgtgc
aaaaggaagccctacctgctgcccagcatccgcgagggcgcgcgcctgggcgtccaggag
tgccgcagccagttccgccacgagcgctgggactgccgcgtggccgccgccccctcggcc
gccagccccctcttcggctacgagctgagcagcggcaccaaggaaacagcgtttatctac
gcggtgatggctgcaggcctggtgcacgctgtgaccaggtcatgcagcgcaggcaacatg
acggagtgttcctgtgacaccaccttgcagaacggcggctcagccagcgaaggctggcac
tgggggggctgctcggatgacgtccagtacggcatgtggttcagcagaaagttcctggac
ttccccatcagaaacaccacgggcagagaaagcaaagtgctgttagcgatgaaccttcat
aacaatgaagctggaaggcaggctgtggccaagctgatgtccgtagactgccgctgccac
ggagtgtccggctcctgtgcggtgaaaacatgctggaaaaccatgtcttcttttgagaag
attggccatttcctgaaggataaatatgagcacagtgttcaagtctcagacaaaatcaaa
aggaaaatgcgcaggagagaaaaggaccagaggaaagtaccgatccgcaaggaggatctg
ctctacatccataagtctcccaactactgtgtagaggataagaaaattgggatcccgggg
acacaaggcagagaatgcaaccgcacgtcggagggcgcgggcggctgcaacctcctctgc
tgtggccgaggctacaacacccacgtggtcagacacgtggagagatgcgagtgcaagttc
atctggtgctgctacgttcgctgcaggaggtgtgaaagcatgactgacgtccacacctgc
aagtaa

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