Vulpes vulpes (red fox): 112914456
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Entry
112914456 CDS
T05911
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
KO
K00572
wingless-type MMTV integration site family, member 7
Organism
vvp
Vulpes vulpes (red fox)
Pathway
vvp04150
mTOR signaling pathway
vvp04310
Wnt signaling pathway
vvp04390
Hippo signaling pathway
vvp04550
Signaling pathways regulating pluripotency of stem cells
vvp04916
Melanogenesis
vvp04934
Cushing syndrome
vvp05010
Alzheimer disease
vvp05022
Pathways of neurodegeneration - multiple diseases
vvp05165
Human papillomavirus infection
vvp05200
Pathways in cancer
vvp05205
Proteoglycans in cancer
vvp05217
Basal cell carcinoma
vvp05224
Breast cancer
vvp05225
Hepatocellular carcinoma
vvp05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
vvp00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
112914456 (WNT7A)
04390 Hippo signaling pathway
112914456 (WNT7A)
04150 mTOR signaling pathway
112914456 (WNT7A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
112914456 (WNT7A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
112914456 (WNT7A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
112914456 (WNT7A)
05205 Proteoglycans in cancer
112914456 (WNT7A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
112914456 (WNT7A)
05226 Gastric cancer
112914456 (WNT7A)
05217 Basal cell carcinoma
112914456 (WNT7A)
05224 Breast cancer
112914456 (WNT7A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
112914456 (WNT7A)
09164 Neurodegenerative disease
05010 Alzheimer disease
112914456 (WNT7A)
05022 Pathways of neurodegeneration - multiple diseases
112914456 (WNT7A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
112914456 (WNT7A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
vvp00536
]
112914456 (WNT7A)
Glycosaminoglycan binding proteins [BR:
vvp00536
]
Heparan sulfate / Heparin
Morphogens
112914456 (WNT7A)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
112914456
NCBI-ProteinID:
XP_025847338
UniProt:
A0A3Q7RQ31
LinkDB
All DBs
Position
Unknown
AA seq
349 aa
AA seq
DB search
MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP
VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ
ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEVYTCK
NT seq
1050 nt
NT seq
+upstream
nt +downstream
nt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcggtggcttctcctccgtggtagctctgggcgcgagcatcatctgtaacaag
atcccgggcctggctcccagacagcgggcgatatgccagagccgccccgacgccatcatc
gtcataggagaaggctcgcaaatgggcctcgacgagtgtcagtttcagttccgcaatggc
cgctggaactgctcagccctgggggagcgcaccgtcttcgggaaggagctcaaagtgggg
agccgggaggctgccttcacctacgccatcatcgctgccggcgtggcccacgccatcacg
gccgcctgcacccaaggcaacctgagtgactgtggctgcgacaaggagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc
ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttgcacaataacgaggcgggccgaaagatcctggaggaaaacatgaagctggagtgc
aagtgccacggtgtgtccggctcgtgcaccaccaagacgtgctggaccacactgccacag
ttccgcgagctgggctacgtgctcaaggacaagtacaacgaggccgtccacgtggagccg
gtgcgcgccagccgcaacaagcggcccaccttcctgaagatcaagaagccgctgtcctac
cgcaagcccatggacacagacctggtgtacatcgagaagtcgcccaactactgcgaggag
gacccggtgacgggcagcgtgggcacgcagggccgcgcctgcaacaagacggccccgcag
gccagcggctgtgacctcatgtgctgcggtcgcggctacaacacccaccagtacgcccgc
gtgtggcagtgcaactgcaagtttcactggtgctgttatgtcaagtgcaacacctgcagc
gagcgtaccgaggtgtacacgtgcaagtga
DBGET
integrated database retrieval system