Macaca mulatta (rhesus monkey): 693419
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Entry
693419 CDS
T01028
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
KO
K00572
wingless-type MMTV integration site family, member 7
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
693419 (WNT7A)
04390 Hippo signaling pathway
693419 (WNT7A)
04150 mTOR signaling pathway
693419 (WNT7A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
693419 (WNT7A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
693419 (WNT7A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
693419 (WNT7A)
05205 Proteoglycans in cancer
693419 (WNT7A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
693419 (WNT7A)
05226 Gastric cancer
693419 (WNT7A)
05217 Basal cell carcinoma
693419 (WNT7A)
05224 Breast cancer
693419 (WNT7A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
693419 (WNT7A)
09164 Neurodegenerative disease
05010 Alzheimer disease
693419 (WNT7A)
05022 Pathways of neurodegeneration - multiple diseases
693419 (WNT7A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
693419 (WNT7A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mcc00536
]
693419 (WNT7A)
Glycosaminoglycan binding proteins [BR:
mcc00536
]
Heparan sulfate / Heparin
Morphogens
693419 (WNT7A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
693419
NCBI-ProteinID:
NP_001252867
Ensembl:
ENSMMUG00000018445
UniProt:
F7HEW6
LinkDB
All DBs
Position
2:complement(145213924..145270951)
Genome browser
AA seq
349 aa
AA seq
DB search
MNRKARRCLGHLFLSLGMVYLRIGGFSTVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP
VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPVTGSVGTQGRACNKTAPQ
ASGCDLMCCGRGYNTHQYARVWQCNCKFHWCCYVKCNTCSERTEMYTCK
NT seq
1050 nt
NT seq
+upstream
nt +downstream
nt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcggtggcttctccacagtggtagctctgggcgcaagcatcatctgtaacaag
atcccaggcctagctcctagacagcgggcgatctgccagagccggcccgacgccatcatc
gtcataggagaaggctcgcaaatgggcctggacgagtgtcagtttcagttccgcaatggc
cgctggaactgctctgcactgggagagcgcaccgtctttgggaaggagctgaaagtgggg
agccgggaggctgcgttcacctacgccatcattgctgccggcgtggcccatgccatcaca
gctgcctgtacccagggcaacctaagcgactgtggctgcgacaaagagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc
ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttgcacaataacgaggcaggccgaaagatcctggaggagaacatgaagctggaatgt
aagtgccacggcgtgtcaggctcgtgcaccaccaagacgtgctggaccacactgccacag
tttcgggagctgggctacgtgctcaaggacaagtacaacgaggccgttcacgtggagcct
gtgcgtgccagccgcaacaagaggcccaccttcctgaagatcaagaagccactgtcatac
cgcaagcccatggacacggacctggtgtacatcgagaagtcacccaactactgcgaggag
gacccggtgaccggcagtgtgggcacccagggccgcgcctgcaacaagacggccccccag
gccagcggctgtgacctcatgtgctgtgggcgtggctacaacacccaccagtacgcccgc
gtgtggcagtgcaactgtaagttccactggtgctgctatgtcaagtgcaacacgtgcagc
gagcgcacggagatgtacacgtgcaagtga
DBGET
integrated database retrieval system