Phascolarctos cinereus (koala): 110217115
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Entry
110217115 CDS
T05867
Symbol
WNT9A
Name
(RefSeq) protein Wnt-9a
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
pcw
Phascolarctos cinereus (koala)
Pathway
pcw04150
mTOR signaling pathway
pcw04310
Wnt signaling pathway
pcw04390
Hippo signaling pathway
pcw04550
Signaling pathways regulating pluripotency of stem cells
pcw04916
Melanogenesis
pcw04934
Cushing syndrome
pcw05010
Alzheimer disease
pcw05022
Pathways of neurodegeneration - multiple diseases
pcw05165
Human papillomavirus infection
pcw05200
Pathways in cancer
pcw05205
Proteoglycans in cancer
pcw05217
Basal cell carcinoma
pcw05224
Breast cancer
pcw05225
Hepatocellular carcinoma
pcw05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pcw00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
110217115 (WNT9A)
04390 Hippo signaling pathway
110217115 (WNT9A)
04150 mTOR signaling pathway
110217115 (WNT9A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
110217115 (WNT9A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
110217115 (WNT9A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
110217115 (WNT9A)
05205 Proteoglycans in cancer
110217115 (WNT9A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
110217115 (WNT9A)
05226 Gastric cancer
110217115 (WNT9A)
05217 Basal cell carcinoma
110217115 (WNT9A)
05224 Breast cancer
110217115 (WNT9A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
110217115 (WNT9A)
09164 Neurodegenerative disease
05010 Alzheimer disease
110217115 (WNT9A)
05022 Pathways of neurodegeneration - multiple diseases
110217115 (WNT9A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
110217115 (WNT9A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pcw00536
]
110217115 (WNT9A)
Glycosaminoglycan binding proteins [BR:
pcw00536
]
Heparan sulfate / Heparin
Morphogens
110217115 (WNT9A)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
110217115
NCBI-ProteinID:
XP_020854932
UniProt:
A0A6P5LAH5
LinkDB
All DBs
Position
Unknown
AA seq
368 aa
AA seq
DB search
MLAGQVLVGWLSSSSFALMVLFGSLRPSAAYFGLTGSEPLTILPLTTEMEEAATKAHYKV
CDRLKLEKKQRRMCRRDPGVAETLMEAISMSALECQYQFRFERWNCTLEGRYRASLLKRG
FKETAFLYAISSAGLTHALAKACSAGRLERCTCDEAPDLENREAWQWGGCGDNLKYSNKF
VKEFLGKKSSKDLRARVDFHNNLVGMKVIKAGVETTCKCHGVSGSCTVRTCWRQLSPFHE
VGKQLKQKYEASLKVGSTTNEATGEAGDIPPPRRALGSSGPGSDPLPRTPDLVHLDDSPS
FCLASRFSPGTAGRKCYKDKNCESMCCGRGHNTQSRVVTRPCQCQVRWCCYVECKQCTQR
EEVYTCKD
NT seq
1107 nt
NT seq
+upstream
nt +downstream
nt
atgctggctggacaagtcctggtgggctggctctcttcctcctccttcgcgctgatggtg
ctgttcggctccctccgcccctcggccgcctacttcgggctgacaggcagtgagcccctg
accatcctcccactgacgacagaaatggaggaggctgccacaaaggcccactacaaagtg
tgtgaccggctcaagctggagaagaagcagagacgcatgtgccggcgggatccgggtgtg
gccgagacacttatggaggccatcagcatgagtgccctggagtgccagtaccagttccga
tttgagcgctggaactgtactctggagggtcgatatcgggccagcctgctgaagagaggc
ttcaaggagactgcctttctctatgccatttcctcagccggcctgacccacgccctggct
aaagcatgcagcgctgggcgcctggagcgctgcacctgcgacgaggcgccggacctggag
aaccgggaggcctggcagtgggggggttgcggggacaacctcaagtacagcaacaagttt
gtcaaagagttcctggggaagaagtccagcaaggacctgcgtgcccgtgtggacttccac
aacaatttggtggggatgaaggtgatcaaggctggtgtggagaccacctgcaaatgtcac
ggggtctccggctcgtgcaccgtccgcacctgctggcgccagctctcaccattccacgag
gtgggcaaacagctgaagcagaaatacgaggcctccctcaaggtagggagcaccaccaat
gaggcgacaggtgaggctggagacatcccgcctccgcgaagggccctgggttcttccggg
cccggcagcgaccctctcccgcgcacgccagacctggtgcacttggatgactcccccagc
ttctgcctggcgagccggttctccccgggcacagctggccggaagtgctacaaggacaag
aactgtgagagcatgtgctgtgggcgtgggcacaacacgcagagccgggtggtgactcgg
ccctgccagtgccaggtccgctggtgctgctacgtggagtgcaaacagtgcacccagaga
gaggaagtctacacctgcaaagactga
DBGET
integrated database retrieval system