Pan troglodytes (chimpanzee): 471645
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Entry
471645 CDS
T01005
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a isoform X1
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
ptr
Pan troglodytes (chimpanzee)
Pathway
ptr04150
mTOR signaling pathway
ptr04310
Wnt signaling pathway
ptr04390
Hippo signaling pathway
ptr04550
Signaling pathways regulating pluripotency of stem cells
ptr04916
Melanogenesis
ptr04934
Cushing syndrome
ptr05010
Alzheimer disease
ptr05022
Pathways of neurodegeneration - multiple diseases
ptr05165
Human papillomavirus infection
ptr05200
Pathways in cancer
ptr05205
Proteoglycans in cancer
ptr05217
Basal cell carcinoma
ptr05224
Breast cancer
ptr05225
Hepatocellular carcinoma
ptr05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ptr00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
471645 (WNT8A)
04390 Hippo signaling pathway
471645 (WNT8A)
04150 mTOR signaling pathway
471645 (WNT8A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
471645 (WNT8A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
471645 (WNT8A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
471645 (WNT8A)
05205 Proteoglycans in cancer
471645 (WNT8A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
471645 (WNT8A)
05226 Gastric cancer
471645 (WNT8A)
05217 Basal cell carcinoma
471645 (WNT8A)
05224 Breast cancer
471645 (WNT8A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
471645 (WNT8A)
09164 Neurodegenerative disease
05010 Alzheimer disease
471645 (WNT8A)
05022 Pathways of neurodegeneration - multiple diseases
471645 (WNT8A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
471645 (WNT8A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ptr00536
]
471645 (WNT8A)
Glycosaminoglycan binding proteins [BR:
ptr00536
]
Heparan sulfate / Heparin
Morphogens
471645 (WNT8A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
471645
NCBI-ProteinID:
XP_009448001
Ensembl:
ENSPTRG00000017278
VGNC:
13614
UniProt:
A0A2I3TI13
A0A6D2X9Z4
LinkDB
All DBs
Position
4:135811651..135820133
Genome browser
AA seq
369 aa
AA seq
DB search
MLCCIQCLCLVSPFPTLTPCQGGPHCLIPIHLCLTFSLFGRSVNNFLITGPKAYLTYTTS
VALGAQSGIEECKFQFAWERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYIITK
NCSMGDFENCGCDGSNNGKTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNL
HNNRAGRLAVRATMKRTCKCHGISGSCSIQTCWLQLADFREMGDYLKAKYDQALKIEMDK
RQLRAGNSAEGHWVPAEAFLPSAEAELIFLEESPDYCSCNSSLGIYGTEGRECLQNSHNT
SRWERRSCGRLCTECGLQVEERKTEVISSCNCKFQWCCTVKCDQCRHVVSKYYCARSPGS
AQSLGKGSA
NT seq
1110 nt
NT seq
+upstream
nt +downstream
nt
atgctgtgctgcattcagtgcctctgcctggtaagtcctttcccaaccctcactccttgc
caaggaggcccccattgtctcatccccattcacctctgcctcactttttctctttttggt
aggtcagtgaacaatttcctgataacaggtcccaaggcctatctgacctacacgactagc
gtggccttgggtgcccagagtggcatcgaagagtgcaagttccagtttgcttgggaacgc
tggaactgccctgaaaatgctcttcagctctccacccacaacaggctgagaagtgctacc
agagagacttccttcatacatgctatcagctctgctggagtcatgtacatcatcaccaag
aactgtagcatgggtgacttcgaaaactgtggctgtgatgggtcaaacaatggaaaaaca
ggaggccatggttggatctggggaggctgcagcgacaatgtggaatttggggaaaggatc
tccaaactctttgtggacagtttggagaaggggaaggatgccagagccctgatgaatctt
cacaacaacagggccggcagactggcagtgagagccaccatgaaaaggacatgcaaatgt
catggcatctctgggagctgcagcatacagacatgctggctgcagctggctgacttccgg
gagatgggagactacctaaaggccaagtatgaccaggcactgaaaattgaaatggataag
cggcagctgagagctgggaacagcgccgagggccactgggtgcccgctgaggccttcctt
cctagcgcagaggcggaactgatctttttagaggaatcaccagattactgtagctgcaat
tccagcctgggcatctatggcacagagggtcgtgagtgcctacagaacagccacaacaca
tccaggtgggagcgacgtagctgtgggcgcctgtgcactgagtgtgggctgcaggtggaa
gagaggaaaactgaggtcataagcagctgtaactgcaaattccagtggtgctgtacggtc
aagtgtgaccagtgtaggcatgtggtgagcaagtattactgcgcacgctccccaggcagt
gcccagtccctgggtaagggcagtgcctga
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