Macaca mulatta (rhesus monkey): 713764
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Entry
713764 CDS
T01028
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a
KO
K00714
wingless-type MMTV integration site family, member 8
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
713764 (WNT8A)
04390 Hippo signaling pathway
713764 (WNT8A)
04150 mTOR signaling pathway
713764 (WNT8A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
713764 (WNT8A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
713764 (WNT8A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
713764 (WNT8A)
05205 Proteoglycans in cancer
713764 (WNT8A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
713764 (WNT8A)
05226 Gastric cancer
713764 (WNT8A)
05217 Basal cell carcinoma
713764 (WNT8A)
05224 Breast cancer
713764 (WNT8A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
713764 (WNT8A)
09164 Neurodegenerative disease
05010 Alzheimer disease
713764 (WNT8A)
05022 Pathways of neurodegeneration - multiple diseases
713764 (WNT8A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
713764 (WNT8A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
mcc00536
]
713764 (WNT8A)
Glycosaminoglycan binding proteins [BR:
mcc00536
]
Heparan sulfate / Heparin
Morphogens
713764 (WNT8A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
713764
NCBI-ProteinID:
XP_001112480
Ensembl:
ENSMMUG00000022937
LinkDB
All DBs
Position
6:135475499..135484263
Genome browser
AA seq
351 aa
AA seq
DB search
MGNLSMLWAAVGICCAALSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMHTITKNCSMGDFENCGCDGSKNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC
KCHGISGSCSIQTCWLQLADFREMGDYLKAKYDQALKIEMDKQQLRAGNSAEGHWAPAEA
FLPSAEAELIFLEESPDYCTCNSSLGIYGTEGRECLQNSHNTSRWERRSCGRLCTECGLQ
VEERKTEVIISCNCKFQWCCKVKCDQCTHVVSKYYCTRSSGSAQSLSEGSA
NT seq
1056 nt
NT seq
+upstream
nt +downstream
nt
atggggaacctgtctatgctctgggcagctgtgggcatatgctgtgctgcactcagtgcc
tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctatctgacctacacg
actagcgtggccttgggtgcccagagtggcatcgaggaatgcaagttccagtttgcttgg
gaacgctggaactgccctgaaaatgctcttcagctctccacccacaataggctgagaagt
gccaccagagagacttccttcatacatgctatcagctctgccggagtcatgcacaccatc
accaagaactgtagcatgggtgacttcgaaaactgtggctgtgatgggtcaaaaaatgga
aaaacaggaggccatggctggatctggggaggctgcagcgacaatgtggaatttggggaa
aggatctccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatg
aatcttcacaataacagggccggcagactggcagtgagagccaccatgaaaaggacctgc
aaatgtcatggcatctctgggagctgcagcatacagacgtgctggctgcagctggctgac
ttccgagagatgggagactacctaaaggccaagtatgaccaggcgctgaaaattgaaatg
gataagcagcagctgagagctgggaacagcgccgagggccactgggcacctgctgaggcc
ttccttcctagcgcagaggcggaactgatctttttagaggaatcaccagattactgtacc
tgcaattccagcctaggcatctatggcacagagggtcgtgagtgcctacagaacagccac
aacacatccaggtgggagcgacgtagctgtgggcgcctatgcactgaatgtgggctgcag
gtggaagagaggaaaactgaggtcataatcagctgtaactgcaaattccagtggtgctgt
aaggtcaagtgtgaccagtgtacgcatgtggtgagcaagtattactgcacacgctcctca
ggcagtgcccagtccctgagtgagggcagtgcctga
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