Equus caballus (horse): 100063931
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Entry
100063931 CDS
T01058
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
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
100063931 (WNT2B)
04390 Hippo signaling pathway
100063931 (WNT2B)
04150 mTOR signaling pathway
100063931 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100063931 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100063931 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100063931 (WNT2B)
05205 Proteoglycans in cancer
100063931 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100063931 (WNT2B)
05226 Gastric cancer
100063931 (WNT2B)
05217 Basal cell carcinoma
100063931 (WNT2B)
05224 Breast cancer
100063931 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100063931 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100063931 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
100063931 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100063931 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100063931 (WNT2B)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100063931 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100063931
NCBI-ProteinID:
XP_001495040
Ensembl:
ENSECAG00000004705
VGNC:
25045
UniProt:
A0A9L0SSH8
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Position
5:complement(52556149..52569147)
Genome browser
AA seq
393 aa
AA seq
DB search
MLRPSGAEEAAQLPPRRVRAPVPAPAPRPAAPDGSPASPRLSLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1182 nt
NT seq
+upstream
nt +downstream
nt
atgctgaggccgagtggtgcggaggaagccgcgcagctcccccctcggcgcgtccgcgcc
cctgtccccgcgccggcgcccagacccgcggcccccgacggttcgccggcttcgccccgc
ctgagtcttgcctgtcttctgctgttgctgctgctgactctgccggcccgcgtagacaca
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaatatccctggtctg
gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcagtgggcgag
ggggcccgagaatggatccgagagtgtcaacaccagttccgccaccaccgctggaactgc
accacgctggaccgggaccacactgtctttggccgtgtcatgctcagaagtagccgggag
gcagcatttgtatatgccatctcgtcagcaggggtggtccacgctatcactcgagcctgt
agccagggtgaactaagtgtgtgcagctgtgacccctacacccgtggccgacaccacgac
caacgtggggactttgactggggtggctgtagtgacaacatccactatggtgttcgcttt
gccaaggccttcgtggatgccaaggagaagaggcttaaggatgctcgggccctcatgaac
ttgcataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctggagtgtaag
tgccatggcgtgagtggctcctgtactctgcgcacctgctggcgtgcactctcagacttc
cgccgcacaggtgattacctacggcggcgttatgatggggctgtgcaggtgacagccacg
caggatggtgccaacttcacagcagcccgccaaggctatcgccgtgccaccaggactgac
cttgtctactttgacaactccccagactactgtgtcttggacaaggctgcaggttcccta
ggcactgcaggccgtgtctgcagcaagacatccaaagggacagatggttgtgaaatcatg
tgttgcggccgagggtacgacacaactcgagttacccgagtcacccagtgtgagtgcaaa
ttccactggtgctgtgctgtgcggtgcaaggagtgcagaaacactgtggacgtccatact
tgcaaggcccccaagaaggcagagtggctggaccagacctga
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