Equus caballus (horse): 100072609
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Entry
100072609 CDS
T01058
Symbol
WNT8A
Name
(RefSeq) protein Wnt-8a isoform X3
KO
K00714
wingless-type MMTV integration site family, member 8
Organism
ecb
Equus caballus (horse)
Pathway
ecb04150
mTOR signaling pathway
ecb04310
Wnt signaling pathway
ecb04390
Hippo signaling pathway
ecb04550
Signaling pathways regulating pluripotency of stem cells
ecb04916
Melanogenesis
ecb04934
Cushing syndrome
ecb05010
Alzheimer disease
ecb05022
Pathways of neurodegeneration - multiple diseases
ecb05165
Human papillomavirus infection
ecb05200
Pathways in cancer
ecb05205
Proteoglycans in cancer
ecb05217
Basal cell carcinoma
ecb05224
Breast cancer
ecb05225
Hepatocellular carcinoma
ecb05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ecb00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100072609 (WNT8A)
04390 Hippo signaling pathway
100072609 (WNT8A)
04150 mTOR signaling pathway
100072609 (WNT8A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100072609 (WNT8A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100072609 (WNT8A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100072609 (WNT8A)
05205 Proteoglycans in cancer
100072609 (WNT8A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100072609 (WNT8A)
05226 Gastric cancer
100072609 (WNT8A)
05217 Basal cell carcinoma
100072609 (WNT8A)
05224 Breast cancer
100072609 (WNT8A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100072609 (WNT8A)
09164 Neurodegenerative disease
05010 Alzheimer disease
100072609 (WNT8A)
05022 Pathways of neurodegeneration - multiple diseases
100072609 (WNT8A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100072609 (WNT8A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100072609 (WNT8A)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100072609 (WNT8A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
100072609
NCBI-ProteinID:
XP_014586142
Ensembl:
ENSECAG00000014626
VGNC:
25050
UniProt:
A0A9L0SZV3
LinkDB
All DBs
Position
14:complement(37621943..37628442)
Genome browser
AA seq
352 aa
AA seq
DB search
MGDLFMLRVAVGICYATFSASAWSVNNFLITGPKAYLTYTTSVALGAQSGIEECKFQFAW
ERWNCPENALQLSTHNRLRSATRETSFIHAISSAGVMYTITKNCSMGDFENCGCDESKNG
KTGGHGWIWGGCSDNVEFGERISKLFVDSLEKGKDARALMNLHNNRAGRLAVRATMKRTC
KCHGISGSCSIQTCWLQLADFREMGDYLKAKYDRALKIEMDKRQLRAGNSAEGHWAPTEA
FLPSAEAELIFLEESPDYCTHNSSLGIYGTEGRECLQNSHNTSRWEQHSCGRLCTECGLQ
VEERKTEAISSCNCKFQWCCTVKCDQCRHVVNKYYCTRSPGSAVSWGKGSTR
NT seq
1059 nt
NT seq
+upstream
nt +downstream
nt
atgggggacctgtttatgctaagggtggctgtgggcatatgctatgctaccttcagtgcc
tctgcctggtcagtgaacaatttcctgataacaggtcccaaggcctatctgacctacact
accagtgtggccctgggtgcccagagcggcatcgaggaatgcaagttccaatttgcttgg
gaacgctggaactgccccgaaaatgctctccagctgtccactcacaacaggctgagaagt
gccaccagggagacttccttcattcatgctatcagctctgctggagtcatgtacaccatc
accaagaactgtagcatgggtgactttgaaaactgtggctgtgatgagtcaaaaaatgga
aaaacaggaggccatggctggatctgggggggctgcagtgacaatgtggaatttggggaa
aggatctccaaactctttgtggacagcctggagaagggaaaggatgccagagccctgatg
aatcttcacaacaacagggcgggcaggctggcagtgagagccaccatgaaaaggacctgc
aaatgtcacggcatctcggggagctgcagcatccagacatgctggttgcagctggctgac
ttccgggagatgggagactacctaaaggccaagtatgaccgggcgctgaaaattgagatg
gataaacggcagctaagggctgggaacagcgccgagggccactgggcacccactgaggcc
ttcctcccaagcgcagaggctgaactgatctttttagaggaatcgccagattactgtacc
cacaattctagcctgggcatctatggcacagagggtcgggagtgtctgcagaatagccac
aacacatccaggtgggagcaacacagctgtgggcgcttgtgcaccgaatgtggcctgcag
gtggaagagaggaagactgaagctatcagcagctgtaactgcaaattccagtggtgctgc
acagtgaagtgtgaccagtgtaggcatgtggtgaacaagtactactgtacacgctcccca
ggcagtgctgtgtcctggggcaagggcagcaccagataa
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