Puma concolor (puma): 112861375
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Entry
112861375 CDS
T08890
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
pcoo
Puma concolor (puma)
Pathway
pcoo04150
mTOR signaling pathway
pcoo04310
Wnt signaling pathway
pcoo04390
Hippo signaling pathway
pcoo04550
Signaling pathways regulating pluripotency of stem cells
pcoo04916
Melanogenesis
pcoo04934
Cushing syndrome
pcoo05010
Alzheimer disease
pcoo05022
Pathways of neurodegeneration - multiple diseases
pcoo05165
Human papillomavirus infection
pcoo05200
Pathways in cancer
pcoo05205
Proteoglycans in cancer
pcoo05217
Basal cell carcinoma
pcoo05224
Breast cancer
pcoo05225
Hepatocellular carcinoma
pcoo05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pcoo00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
112861375 (WNT8A)
04390 Hippo signaling pathway
112861375 (WNT8A)
04150 mTOR signaling pathway
112861375 (WNT8A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
112861375 (WNT8A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
112861375 (WNT8A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
112861375 (WNT8A)
05205 Proteoglycans in cancer
112861375 (WNT8A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
112861375 (WNT8A)
05226 Gastric cancer
112861375 (WNT8A)
05217 Basal cell carcinoma
112861375 (WNT8A)
05224 Breast cancer
112861375 (WNT8A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
112861375 (WNT8A)
09164 Neurodegenerative disease
05010 Alzheimer disease
112861375 (WNT8A)
05022 Pathways of neurodegeneration - multiple diseases
112861375 (WNT8A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
112861375 (WNT8A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pcoo00536
]
112861375 (WNT8A)
Glycosaminoglycan binding proteins [BR:
pcoo00536
]
Heparan sulfate / Heparin
Morphogens
112861375 (WNT8A)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
112861375
NCBI-ProteinID:
XP_025780516
UniProt:
A0A6P6HY46
LinkDB
All DBs
Position
Unknown
AA seq
343 aa
AA seq
DB search
MGDLFMLRVAVGICYATFSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYTITKNCSMGDFENCGCDESKNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRAIMKRTC
KCHGISGSCSIQTCWLQLADFREMGDYLKAKYERALKIEMDKRQLRAGNSAEGHWAPTEG
FLPSAEAELIFLEESPDYCTRNSSLGIYGTEGRECLQNSHNTSRWEQRSCGRLCTECGLQ
VEERRTEAISSCNCKFQWCCTVRCDQCRHVVNKYYCTSSPGSA
NT seq
1032 nt
NT seq
+upstream
nt +downstream
nt
atgggagacctgtttatgctcagggtggctgttggcatatgttatgccaccttcagtgcc
tctgcatggtcagtgaacaatttcctgataacaggccctaaggcctatctgacctacact
actagtgtggccctgggtgcccagagtggcattgaggagtgtaagttccaatttgcttgg
gaacgctggaactgcccggaaaatgctctccagctgtccactcacaacaggttgagaagc
gccaccagggagacttccttcattcatgcaatcagctctgctggagtcatgtacaccatc
accaagaactgtagcatgggtgactttgaaaactgtggctgtgatgagtcaaaaaatgga
aaaacaggaggtcatggctggatctggggaggctgcagcgacaatgtggaatttggggaa
aggatctccaaactctttgtggacagcctggaaaagggaaaggatgccagagccctgatg
aatcttcacaacaatagggcaggcaggctggcagtgagagccattatgaaaaggacctgc
aaatgtcatggcatctctggaagctgcagtatccagacatgctggctgcagctggctgac
ttccgggagatgggagactacctgaaggccaagtacgaacgggccctgaaaatcgagatg
gataagcggcagttaagggctgggaacagtgctgagggccactgggcacccactgaggga
ttccttcctagtgcagaggctgagctgatctttttggaggaatcaccagattactgtacc
cgcaattccagcctgggcatctatggcacagaaggtcgggagtgtctacagaatagccac
aacacatccaggtgggagcaacgcagctgtgggcgcttgtgcaccgagtgtggcctgcag
gtggaggagagaagaactgaggctatcagcagctgtaactgcaaattccagtggtgttgc
acagtcaggtgtgaccagtgtaggcatgtggtaaacaagtactactgcacaagttcccca
ggcagtgcttga
DBGET
integrated database retrieval system