Macaca mulatta (rhesus monkey): 696326
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Entry
696326 CDS
T01028
Symbol
WNT9A
Name
(RefSeq) protein Wnt-9a isoform X1
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc04150
mTOR signaling pathway
mcc04310
Wnt signaling pathway
mcc04390
Hippo signaling pathway
mcc04550
Signaling pathways regulating pluripotency of stem cells
mcc04916
Melanogenesis
mcc04934
Cushing syndrome
mcc05010
Alzheimer disease
mcc05022
Pathways of neurodegeneration - multiple diseases
mcc05165
Human papillomavirus infection
mcc05200
Pathways in cancer
mcc05205
Proteoglycans in cancer
mcc05217
Basal cell carcinoma
mcc05224
Breast cancer
mcc05225
Hepatocellular carcinoma
mcc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
696326 (WNT9A)
04390 Hippo signaling pathway
696326 (WNT9A)
04150 mTOR signaling pathway
696326 (WNT9A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
696326 (WNT9A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
696326 (WNT9A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
696326 (WNT9A)
05205 Proteoglycans in cancer
696326 (WNT9A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
696326 (WNT9A)
05226 Gastric cancer
696326 (WNT9A)
05217 Basal cell carcinoma
696326 (WNT9A)
05224 Breast cancer
696326 (WNT9A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
696326 (WNT9A)
09164 Neurodegenerative disease
05010 Alzheimer disease
696326 (WNT9A)
05022 Pathways of neurodegeneration - multiple diseases
696326 (WNT9A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
696326 (WNT9A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mcc00536
]
696326 (WNT9A)
Glycosaminoglycan binding proteins [BR:
mcc00536
]
Heparan sulfate / Heparin
Morphogens
696326 (WNT9A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
696326
NCBI-ProteinID:
XP_014970078
Ensembl:
ENSMMUG00000008338
UniProt:
A0A5F8AIA3
LinkDB
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Position
1:complement(85514927..85544619)
Genome browser
AA seq
394 aa
AA seq
DB search
MCRGPRPFSPPPPLPAHPGFFLPLSPPDGHACPLSPGHRDTWPGSSRASWRWAHTGLSVP
RLTGSEPLTVLPLTLEPEAAAQAHYKACDRLKLERKQRRMCRRDPGVAETLVEAVSMSAL
ECQFQFRFERWNCTLEGRYRASLLKRGFKETAFLYAISSAGLTHALAKACSAGRMERCTC
DEAPDLENREAWQWGGCGDNLKYSSKFVKEFLGRRSSKDLRARVDFHNNLVGVKVIKAGV
ETTCKCHGVSGSCTVRTCWRQLAPFHEVGKHLKHKYETALKVGSTTNEAAGEAGAISPPR
GRASGVGGSDPLPRTPELVHLDDSPSFCLAGRFSPGTAGRRCHREKNCESICCGRGHNTQ
SRVVTRPCQCQVRWCCYVECRQCTQREEVYTCKG
NT seq
1185 nt
NT seq
+upstream
nt +downstream
nt
atgtgcagggggccaaggcccttctcacctccccctcccctgcctgctcatcctggattc
tttctgcccctctcacccccggatggacatgcctgtcccctgtcccctggccaccgagac
acctggccaggctccagcagggcttcctggcgctgggctcacactggcctctctgtgccc
aggctgacgggcagcgagcccctgaccgtcctcccgctgaccctggagcccgaggcggcc
gcccaggcacactacaaggcctgcgaccggctgaagctggagcggaagcagcggcgcatg
tgccgccgggacccgggtgtggcagagacgctggtggaggccgtgagcatgagtgcgctt
gagtgccagttccaattccgctttgagcgctggaactgcacgctggagggccgctaccgg
gccagcctgctcaagcgaggcttcaaggagactgccttcctctatgccatctcctcggct
ggcctgacgcacgcactggccaaggcatgcagcgcgggccgcatggagcgctgtacctgc
gatgaggcgcccgacctggagaaccgtgaggcctggcagtgggggggctgcggagacaac
ctcaagtacagcagcaagtttgtcaaggagttcctgggcagacggtcaagcaaggatctg
cgagcccgtgtggacttccacaacaacctcgtgggtgtgaaggtgatcaaggctggggtg
gagaccacctgcaagtgccacggcgtatcaggctcatgcacggtgcggacctgctggcgg
cagctggcgcccttccatgaggtgggcaagcacctgaagcacaagtacgagacagcactc
aaggtgggcagcaccaccaatgaagcggcaggtgaggcaggtgccatttccccaccacgg
ggccgtgcctcgggggtgggcggcagtgacccgctaccccgcactccagagctggtgcac
ctggacgactcgcctagcttctgcctggccggccgcttctccccgggcaccgctggccgt
agatgccaccgtgagaagaactgtgagagcatctgctgcggccgcggccataacacacag
agccgggtggtgacgaggccctgccagtgccaggtgcgttggtgctgctatgtggagtgc
aggcagtgcacacagcgtgaggaggtctacacctgcaagggctga
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