Trachypithecus francoisi (Francois's langur): 117073269
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Entry
117073269 CDS
T07225
Symbol
WNT16
Name
(RefSeq) protein Wnt-16
KO
K01558
wingless-type MMTV integration site family, member 16
Organism
tfn
Trachypithecus francoisi (Francois's langur)
Pathway
tfn04150
mTOR signaling pathway
tfn04310
Wnt signaling pathway
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Hippo signaling pathway
tfn04550
Signaling pathways regulating pluripotency of stem cells
tfn04916
Melanogenesis
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Cushing syndrome
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Alzheimer disease
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Pathways of neurodegeneration - multiple diseases
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Human papillomavirus infection
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Pathways in cancer
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Transcriptional misregulation in cancer
tfn05205
Proteoglycans in cancer
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Basal cell carcinoma
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Breast cancer
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Hepatocellular carcinoma
tfn05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
tfn00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
117073269 (WNT16)
04390 Hippo signaling pathway
117073269 (WNT16)
04150 mTOR signaling pathway
117073269 (WNT16)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
117073269 (WNT16)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
117073269 (WNT16)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
117073269 (WNT16)
05202 Transcriptional misregulation in cancer
117073269 (WNT16)
05205 Proteoglycans in cancer
117073269 (WNT16)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
117073269 (WNT16)
05226 Gastric cancer
117073269 (WNT16)
05217 Basal cell carcinoma
117073269 (WNT16)
05224 Breast cancer
117073269 (WNT16)
09172 Infectious disease: viral
05165 Human papillomavirus infection
117073269 (WNT16)
09164 Neurodegenerative disease
05010 Alzheimer disease
117073269 (WNT16)
05022 Pathways of neurodegeneration - multiple diseases
117073269 (WNT16)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
117073269 (WNT16)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
tfn00536
]
117073269 (WNT16)
Glycosaminoglycan binding proteins [BR:
tfn00536
]
Heparan sulfate / Heparin
Morphogens
117073269 (WNT16)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
117073269
NCBI-ProteinID:
XP_033049809
LinkDB
All DBs
Position
Unknown
AA seq
365 aa
AA seq
DB search
MDRAALLGLARLCALWAALLVLFPYGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KRKPYLLPSIREGARLGIQECRSQFRHERWNCMITAAATTAPMGASPLFGYELSSGTKET
AFIYAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSR
KFLDFPIRNTTGKENKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMS
SFEKIGHLLKDKYENSIQISDKIKRKMRRREKDQRKIPIHKDDLLYVNKSPNYCVEDKKL
GIPGTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTD
VHTCK
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atggacagggcggcgctcctgggactggcccgcctgtgcgccctgtgggcagccctgctc
gtgctgttcccctacggagcccaaggaaactggatgtggttgggcattgcctccttcggg
gttccagagaagctgggctgcgccaatttaccgctgaacagccgccagaaggagctgtgc
aagaggaagccgtacctgctgccgagcatccgagagggcgcccggctgggcattcaggag
tgcaggagtcagttcagacacgagagatggaactgcatgatcaccgctgccgccaccacc
gccccgatgggcgccagccccctctttggctacgagctgagcagcggcaccaaagagaca
gcatttatttatgctgttatggctgcaggcctggtgcattctgtgaccaggtcatgcagt
gcaggcaacatgacagagtgttcctgtgacaccaccttgcagaacggcggctcagcaagt
gaaggatggcactgggggggctgctccgatgatgtccagtatggcatgtggttcagcaga
aagttcctagatttccccatcagaaacaccacgggcaaagaaaacaaagtactattagca
atgaacctacataacaatgaagctggaaggcaggctgtcgccaagttgatgtcagtagac
tgccgctgccacggagtttccggctcctgtgctgtgaaaacatgctggaaaaccatgtct
tcttttgaaaagattggccatttgttgaaggataaatatgaaaacagtatccaaatatca
gacaaaataaagaggaaaatgcgcaggagagaaaaagatcagaggaaaataccaatccac
aaggatgatctgctctatgttaataagtctcccaactactgtgtagaagataagaaactg
ggaatcccagggacacaaggcagagaatgcaaccgtacatcagaaggtgcagatggctgc
aacctcctctgctgtggccgaggttacaacacccacgtggtccggcacgtggagaggtgt
gagtgtaagtttatctggtgctgctatgtccgttgcaggaggtgtgaaagcatgactgat
gtccacacttgcaagtaa
DBGET
integrated database retrieval system