Macaca mulatta (rhesus monkey): 713864
Help
Entry
713864 CDS
T01028
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X2
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
713864 (WNT7B)
04390 Hippo signaling pathway
713864 (WNT7B)
04150 mTOR signaling pathway
713864 (WNT7B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
713864 (WNT7B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
713864 (WNT7B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
713864 (WNT7B)
05205 Proteoglycans in cancer
713864 (WNT7B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
713864 (WNT7B)
05226 Gastric cancer
713864 (WNT7B)
05217 Basal cell carcinoma
713864 (WNT7B)
05224 Breast cancer
713864 (WNT7B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
713864 (WNT7B)
09164 Neurodegenerative disease
05010 Alzheimer disease
713864 (WNT7B)
05022 Pathways of neurodegeneration - multiple diseases
713864 (WNT7B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
713864 (WNT7B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mcc00536
]
713864 (WNT7B)
Glycosaminoglycan binding proteins [BR:
mcc00536
]
Heparan sulfate / Heparin
Morphogens
713864 (WNT7B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
713864
NCBI-ProteinID:
XP_001110372
Ensembl:
ENSMMUG00000000180
UniProt:
F7HJM7
LinkDB
All DBs
Position
10:5524265..5580853
Genome browser
AA seq
349 aa
AA seq
DB search
MHRNFRKWIFYVFLCFGVLYVKLGALSSVVALGANIICNKIPGLAPRQRAICQSRPDAII
VIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHAVT
AACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARRLM
NLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAVQVEV
VRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPG
ADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq
1050 nt
NT seq
+upstream
nt +downstream
nt
atgcacagaaactttcgcaagtggattttctacgtgtttctctgctttggcgtcctgtac
gtgaagctcggagcactgtcatcagtggtggccctgggagccaacatcatctgcaacaag
attcctggcctagccccgcggcagcgtgccatctgccagagccggcccgatgccatcatt
gtgatcggggagggggcgcagatgggcatcaacgagtgccagtaccagttccgctttgga
cgctggaactgctctgccctcggcgagaagactgtctttgggcaagagctccgagtaggg
agccgtgaggctgccttcacgtatgccatcaccgcggctggcgtagcgcacgccgtcact
gctgcctgcagccaaggcaacctgagcaactgcggctgtgaccgagagaagcagggctac
tacaaccaggccgagggctggaagtggggtggctgctcggccgacgtgcgttacggcatc
gacttctcccggcgcttcgtggacgctcgggagatcaagaagaacgcgcggcgcctcatg
aacctgcacaacaatgaggccggcaggaaggttctggaggaccgaatgcagctggagtgc
aagtgtcacggcgtgtctggctcctgcaccaccaagacctgctggaccacgctgcctaag
ttccgagaggtgggccacctgctgaaggagaagtacaacgcggccgtgcaggtggaggtg
gtgcgggccagccgcctgcggcagcccaccttcctgcgcatcaaacagctgcgcagctat
cagaagcccatggagacggacctggtgtacatcgagaagtcacccaactactgcgaggag
gacgcggccacgggcagcgtgggcacgcagggccgcctctgcaaccgcacgtcgcccggt
gcggacggctgtgacaccatgtgctgtggccgaggctacaacactcaccagtacaccaag
gtgtggcagtgcaactgcaaattccactggtgctgcttcgtcaagtgcaacacctgcagc
gagcgcaccgaggtcttcacctgcaagtga
DBGET
integrated database retrieval system