Mus musculus (house mouse): 216795
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Entry
216795 CDS
T01002
Symbol
Wnt9a, Wnt14, wnt-14
Name
(RefSeq) wingless-type MMTV integration site family, member 9A
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
mmu
Mus musculus (house mouse)
Pathway
mmu04150
mTOR signaling pathway
mmu04310
Wnt signaling pathway
mmu04390
Hippo signaling pathway
mmu04550
Signaling pathways regulating pluripotency of stem cells
mmu04916
Melanogenesis
mmu04934
Cushing syndrome
mmu05010
Alzheimer disease
mmu05022
Pathways of neurodegeneration - multiple diseases
mmu05165
Human papillomavirus infection
mmu05200
Pathways in cancer
mmu05205
Proteoglycans in cancer
mmu05217
Basal cell carcinoma
mmu05224
Breast cancer
mmu05225
Hepatocellular carcinoma
mmu05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
mmu00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
216795 (Wnt9a)
04390 Hippo signaling pathway
216795 (Wnt9a)
04150 mTOR signaling pathway
216795 (Wnt9a)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
216795 (Wnt9a)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
216795 (Wnt9a)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
216795 (Wnt9a)
05205 Proteoglycans in cancer
216795 (Wnt9a)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
216795 (Wnt9a)
05226 Gastric cancer
216795 (Wnt9a)
05217 Basal cell carcinoma
216795 (Wnt9a)
05224 Breast cancer
216795 (Wnt9a)
09172 Infectious disease: viral
05165 Human papillomavirus infection
216795 (Wnt9a)
09164 Neurodegenerative disease
05010 Alzheimer disease
216795 (Wnt9a)
05022 Pathways of neurodegeneration - multiple diseases
216795 (Wnt9a)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
216795 (Wnt9a)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mmu00536
]
216795 (Wnt9a)
Glycosaminoglycan binding proteins [BR:
mmu00536
]
Heparan sulfate / Heparin
Morphogens
216795 (Wnt9a)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
216795
NCBI-ProteinID:
NP_647459
MGI:
2446084
Ensembl:
ENSMUSG00000000126
UniProt:
Q8R5M2
LinkDB
All DBs
Position
11:59197675..59224378
Genome browser
AA seq
365 aa
AA seq
DB search
MLDGSLLARWLAAAFGLTLLLAALRPSAAYFGLTGSEPLTILPLTLETEAAAQAHYKACD
RLKLERKQRRMCRRDPGVAETLVEAVSMSALECQYQFRFERWNCTLEGRYRASLLKRGFK
ETAFLYAISSAGLTHALAKACSAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVK
EFLGRRSSKDLRARVDFHNNLVGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVG
KHLKHKYETSLKVGSTTNEATGEAGAISPPRGRASGSGGGDPLPRTPELVHLDDSPSFCL
AGRFSPGTAGRRCHREKNCESICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEV
YTCKG
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctggatgggtcccttctggcgcgctggctggccgcggccttcgggctgacgctgctg
ctcgccgcgctgcgcccttcggccgcctacttcgggctaacaggcagtgaacccctgact
atcctccctctgaccctggagaccgaggctgcggcccaagcacactacaaggcctgcgac
aggctgaagctggagcgcaagcagcgccgcatgtgccgcagggacccgggtgtggccgag
acactggtggaggccgtaagcatgagtgccctggagtgccagtaccagttccgctttgag
cgctggaactgcaccctggagggccgctaccgagccagcctgctcaagcgaggcttcaag
gagactgctttcctctacgccatctcttctgccggcctgacgcatgcactggccaaggcc
tgcagtgcaggccgcatggagcgctgcacgtgtgatgaggcacccgacctggaaaaccgc
gaggcctggcagtggggcggctgcggggacaacctcaagtacagcagcaagtttgtcaag
gagttcctgggccggcgctctagcaaggatttgcgagcccgagtggacttccacaacaac
ctcgtgggtgtgaaggtgataaaggctggagtggaaaccacttgcaaatgccatggtgtg
tctggctcctgcaccgtgcggacctgctggcggcagctagcacccttccacgaggtgggc
aagcacctaaaacacaaatatgagacctcgctcaaggtgggcagcactaccaatgaagcc
actggagaggcaggtgccatctccccaccgcggggccgggcttctgggtcaggaggtggc
gacccactgccccgaacaccagagcttgtacacctggacgactctcccagcttctgcctg
gctggccgcttttcccctggcacggcaggccgcaggtgtcaccgggagaagaactgtgag
agtatttgttgtggccgaggccacaacacacagagtcgtgtggtgacaaggccctgccaa
tgccaggtccgctggtgctgctacgtggagtgcaggcagtgtacacagagagaggaggtc
tatacctgcaagggctga
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integrated database retrieval system
