Equus caballus (horse): 100055450
Help
Entry
100055450 CDS
T01058
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
KO
K00572
wingless-type MMTV integration site family, member 7
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
100055450 (WNT7A)
04390 Hippo signaling pathway
100055450 (WNT7A)
04150 mTOR signaling pathway
100055450 (WNT7A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100055450 (WNT7A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100055450 (WNT7A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100055450 (WNT7A)
05205 Proteoglycans in cancer
100055450 (WNT7A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100055450 (WNT7A)
05226 Gastric cancer
100055450 (WNT7A)
05217 Basal cell carcinoma
100055450 (WNT7A)
05224 Breast cancer
100055450 (WNT7A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100055450 (WNT7A)
09164 Neurodegenerative disease
05010 Alzheimer disease
100055450 (WNT7A)
05022 Pathways of neurodegeneration - multiple diseases
100055450 (WNT7A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100055450 (WNT7A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100055450 (WNT7A)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100055450 (WNT7A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100055450
NCBI-ProteinID:
XP_023475667
Ensembl:
ENSECAG00000009213
VGNC:
25048
LinkDB
All DBs
Position
16:complement(4244557..4269166)
Genome browser
AA seq
246 aa
AA seq
DB search
MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKVGGQEGSRAAPAEMPQGSLFRMAGVGSPVVSHRALHTASFCLTLLSVRCW
SGFVGA
NT seq
741 nt
NT seq
+upstream
nt +downstream
nt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcggcggcttctcctccgtggtagctctgggtgcgagcatcatctgtaacaag
atcccaggcctggctcccagacagcgggcgatctgccagagccggcccgacgccatcatc
gtcataggagaaggctcgcaaatgggccttgacgagtgtcagtttcagttccgcaatggc
cgctggaactgctcggcgctgggggagcgcaccgtcttcgggaaggagctcaaagtgggg
agccgggaggctgcctttacgtacgccatcattgctgccggagtggcccacgccatcaca
gcggcctgcacccagggcaacctgagcgactgtggctgcgacaaggagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctacggcatc
ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttacacaataacgaggcaggccgaaaggtaggcggccaggaggggagccgggcggct
ccggcagagatgccgcagggttccttattcagaatggctggtgtcgggtctcctgtggtg
agccacagggctctgcacacagcctcattctgcttgactctgttgtcagttcgctgctgg
tcaggatttgtgggtgcgtga
DBGET
integrated database retrieval system