Pan troglodytes (chimpanzee): 469697
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Entry
469697 CDS
T01005
Symbol
WNT9A
Name
(RefSeq) protein Wnt-9a isoform X2
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
ptr
Pan troglodytes (chimpanzee)
Pathway
ptr04150
mTOR signaling pathway
ptr04310
Wnt signaling pathway
ptr04390
Hippo signaling pathway
ptr04550
Signaling pathways regulating pluripotency of stem cells
ptr04916
Melanogenesis
ptr04934
Cushing syndrome
ptr05010
Alzheimer disease
ptr05022
Pathways of neurodegeneration - multiple diseases
ptr05165
Human papillomavirus infection
ptr05200
Pathways in cancer
ptr05205
Proteoglycans in cancer
ptr05217
Basal cell carcinoma
ptr05224
Breast cancer
ptr05225
Hepatocellular carcinoma
ptr05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ptr00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
469697 (WNT9A)
04390 Hippo signaling pathway
469697 (WNT9A)
04150 mTOR signaling pathway
469697 (WNT9A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
469697 (WNT9A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
469697 (WNT9A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
469697 (WNT9A)
05205 Proteoglycans in cancer
469697 (WNT9A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
469697 (WNT9A)
05226 Gastric cancer
469697 (WNT9A)
05217 Basal cell carcinoma
469697 (WNT9A)
05224 Breast cancer
469697 (WNT9A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
469697 (WNT9A)
09164 Neurodegenerative disease
05010 Alzheimer disease
469697 (WNT9A)
05022 Pathways of neurodegeneration - multiple diseases
469697 (WNT9A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
469697 (WNT9A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ptr00536
]
469697 (WNT9A)
Glycosaminoglycan binding proteins [BR:
ptr00536
]
Heparan sulfate / Heparin
Morphogens
469697 (WNT9A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
469697
NCBI-ProteinID:
XP_016795686
Ensembl:
ENSPTRG00000002062
VGNC:
9403
LinkDB
All DBs
Position
1:21413396..21443012
Genome browser
AA seq
295 aa
AA seq
DB search
MCRRDPGVAETLVEAVSMSALECQFQFRFERWNCTLEGRYRASLLKRGFKETAFLYAISS
AGLTHALAKACSAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVKEFLGRRSSKD
LRARVDFHNNLVGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVGKHLKHKYETA
LKVGSTTNEAAGEAGAISPPRGRASGAGGSDPLPRTPELVHLDDSPSFCLAGRFSPGTAG
RRCHREKNCESICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEVYTCKG
NT seq
888 nt
NT seq
+upstream
nt +downstream
nt
atgtgccgccgggacccgggcgtggcagagacgctggtggaggccgtgagcatgagtgcg
ctcgagtgccagttccagttccgctttgagcgctggaactgcacgctggagggccgctac
cgggccagcctgctcaagcgaggcttcaaggagactgccttcctctatgccatctcctcg
gctggcctgacgcacgcactggccaaggcatgcagcgcgggccgcatggagcgctgtacc
tgcgatgaggcgcccgacctggagaaccgtgaggcctggcagtgggggggctgcggagac
aaccttaagtacagcagcaagttcgtcaaggaattcctgggcagacggtcaagcaaggat
ctgcgagcccgtgtggacttccacaacaacctcgtgggtgtgaaggtgatcaaggctggg
gtggagaccacctgcaagtgccatggcgtgtcaggctcatgcacggtgcggacctgctgg
cggcagttggcgcctttccatgaggtgggcaagcatctgaagcacaagtatgagacggca
ctcaaggtgggcagcaccaccaatgaagctgccggcgaggcaggtgccatctccccacca
cggggccgtgcctcgggggcaggcggcagcgacccgctgccccgcactccagagctggtg
cacctggatgactcgcctagcttctgcctggctggccgcttctccccgggcaccgctggc
cgtaggtgccaccgtgagaagaactgcgagagcatctgctgcggccgcggccataacaca
cagagccgggtggtgacaaggccctgccagtgccaggtgcgttggtgctgctatgtggag
tgcaggcagtgcacgcagcgtgaggaggtctacacctgcaagggctga
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