Entry |
|
Symbol |
WNT16
|
Name |
(RefSeq) Wnt family member 16
|
KO |
K01558 | wingless-type MMTV integration site family, member 16 |
|
Organism |
|
Pathway |
hsa04550 | Signaling pathways regulating pluripotency of stem cells |
hsa05022 | Pathways of neurodegeneration - multiple diseases |
hsa05202 | Transcriptional misregulation in cancer |
|
Network |
|
Element |
N00010 | Mutation-inactivated PTCH1 to Hedgehog signaling pathway |
N00017 | Mutation-activated SMO to Hedgehog signaling pathway |
N00059 | FZD7-overexpression to Wnt signaling pathway |
N00060 | LRP6-overexpression to Wnt signaling pathway |
N00117 | E2A-PBX1 fusion to transcriptional activation |
N01442 | Wnt signaling modulation, Wnt inhibitor |
N01443 | Wnt signaling modulation, Wnt acylation |
|
Brite |
KEGG Orthology (KO) [BR:hsa00001]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
51384 (WNT16)
04390 Hippo signaling pathway
51384 (WNT16)
04150 mTOR signaling pathway
51384 (WNT16)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
51384 (WNT16)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
51384 (WNT16)
05202 Transcriptional misregulation in cancer
51384 (WNT16)
05205 Proteoglycans in cancer
51384 (WNT16)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
51384 (WNT16)
05226 Gastric cancer
51384 (WNT16)
05217 Basal cell carcinoma
51384 (WNT16)
05224 Breast cancer
51384 (WNT16)
09172 Infectious disease: viral
05165 Human papillomavirus infection
51384 (WNT16)
09164 Neurodegenerative disease
05010 Alzheimer disease
51384 (WNT16)
05022 Pathways of neurodegeneration - multiple diseases
51384 (WNT16)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
51384 (WNT16)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:hsa00536]
51384 (WNT16)
Glycosaminoglycan binding proteins [BR:hsa00536]
Heparan sulfate / Heparin
Morphogens
51384 (WNT16)
|
SSDB |
|
Motif |
|
Other DBs |
|
LinkDB |
|
Position |
7:121325367..121341104
|
AA seq |
365 aa
MDRAALLGLARLCALWAALLVLFPYGAQGNWMWLGIASFGVPEKLGCANLPLNSRQKELC
KRKPYLLPSIREGARLGIQECGSQFRHERWNCMITAAATTAPMGASPLFGYELSSGTKET
AFIYAVMAAGLVHSVTRSCSAGNMTECSCDTTLQNGGSASEGWHWGGCSDDVQYGMWFSR
KFLDFPIGNTTGKENKVLLAMNLHNNEAGRQAVAKLMSVDCRCHGVSGSCAVKTCWKTMS
SFEKIGHLLKDKYENSIQISDKTKRKMRRREKDQRKIPIHKDDLLYVNKSPNYCVEDKKL
GIPGTQGRECNRTSEGADGCNLLCCGRGYNTHVVRHVERCECKFIWCCYVRCRRCESMTD
VHTCK |
NT seq |
1098 nt +upstreamnt +downstreamnt
atggacagggcggcgctcctgggactggcccgcttgtgcgcgctgtgggcagccctgctc
gtgctgttcccctacggagcccaaggaaactggatgtggttgggcattgcctccttcggg
gttccagagaagctgggctgcgccaatttgccgctgaacagccgccagaaggagctgtgc
aagaggaaaccgtacctgctgccgagcatccgagagggcgcccggctgggcattcaggag
tgcgggagccagttcagacacgagagatggaactgcatgatcaccgccgccgccactacc
gccccgatgggcgccagccccctctttggctacgagctgagcagcggcaccaaagagaca
gcatttatttatgctgtgatggctgcaggcctggtgcattctgtgaccaggtcatgcagt
gcaggcaacatgacagagtgttcctgtgacaccaccttgcagaacggcggctcagcaagt
gaaggctggcactgggggggctgctccgatgatgtccagtatggcatgtggttcagcaga
aagttcctagatttccccatcggaaacaccacgggcaaagaaaacaaagtactattagca
atgaacctacataacaatgaagctggaaggcaggctgtcgccaagttgatgtcagtagac
tgccgctgccacggagtttccggctcctgtgctgtgaaaacatgctggaaaaccatgtct
tcttttgaaaagattggccatttgttgaaggataaatatgaaaacagtatccagatatca
gacaaaacaaagaggaaaatgcgcaggagagaaaaagatcagaggaaaataccaatccat
aaggatgatctgctctatgttaataagtctcccaactactgtgtagaagataagaaactg
ggaatcccagggacacaaggcagagaatgcaaccgtacatcagagggtgcagatggctgc
aacctcctctgctgtggccgaggttacaacacccatgtggtcaggcacgtggagaggtgt
gagtgtaagttcatctggtgctgctatgtccgttgcaggaggtgtgaaagcatgactgat
gtccacacttgcaagtaa |