Equus caballus (horse): 100056092
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Entry
100056092 CDS
T01058
Symbol
WNT2
Name
(RefSeq) protein Wnt-2 precursor
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
100056092 (WNT2)
04390 Hippo signaling pathway
100056092 (WNT2)
04150 mTOR signaling pathway
100056092 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100056092 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100056092 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100056092 (WNT2)
05205 Proteoglycans in cancer
100056092 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100056092 (WNT2)
05226 Gastric cancer
100056092 (WNT2)
05217 Basal cell carcinoma
100056092 (WNT2)
05224 Breast cancer
100056092 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100056092 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
100056092 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
100056092 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100056092 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ecb00536
]
100056092 (WNT2)
Glycosaminoglycan binding proteins [BR:
ecb00536
]
Heparan sulfate / Heparin
Morphogens
100056092 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100056092
NCBI-ProteinID:
NP_001107622
Ensembl:
ENSECAG00000024641
VGNC:
25044
UniProt:
Q2QLA5
LinkDB
All DBs
Position
4:complement(74570722..74613286)
Genome browser
AA seq
360 aa
AA seq
DB search
MNAPLGGIWLWLPLLLTWLTPEVSSSWWYMRATGGASRVMCDNVPGLVSRQRQLCHRHPD
VMRAIGLGVAEWTAECQHQFRQHRWNCNTLDRDHSLFGRVLLRSSRESAFVYAISSAGVV
FAITRACSQGELRSCSCDPKKKGTAKDSKGTFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG
AIQVVMNQDGTGFTVANKKFKKPTKNDLVYFENSPDYCIRDRDAGSLGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSRVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPKSADWASPT
NT seq
1083 nt
NT seq
+upstream
nt +downstream
nt
atgaacgcccctctcggtggaatctggctctggctccctctgctcttgacctggctcacc
cctgaggtcagctcttcatggtggtacatgagagctacaggcggggcctccagggtgatg
tgtgacaatgtgccaggtctggtgagccgccagcggcagctgtgccaccgacacccagac
gtgatgcgtgccattggcctgggcgtggccgagtggacagcagagtgccaacaccagttc
cgccagcaccgctggaactgcaacaccctggacagggatcacagcctcttcggcagggtc
ctgctccgaagtagtcgggaatctgcctttgtttacgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaattaagatcctgttcctgtgatccaaag
aagaaggggaccgccaaggacagcaagggcactttcgattggggtggctgcagtgataac
attgactatgggatcaaatttgcccgagcgtttgtggatgccaaggaaaggaaaggaaag
gatgccagagccctgatgaatcttcacaacaacagagccggcaggaaggctgtaaagcgg
ttcttgaaacaagagtgcaagtgtcatggagtgagcggctcgtgcactctgaggacgtgc
tggctggccatggccgacttcagaaaaacgggcgattatctctggaggaagtacaatggg
gccatccaggttgtcatgaaccaggatggcactggtttcactgtggctaacaagaagttt
aagaagccaacaaaaaatgaccttgtgtattttgagaattctccagactactgtatcagg
gaccgggatgcaggctccctgggtacagcaggccgcgtgtgcaacctgacttcccgaggc
atggacagctgcgaagtcatgtgctgcgggagaggctacgacacttcccgtgtcacccgg
atgaccaagtgtgagtgtaagttccattggtgctgtgctgtgcgctgtcaggactgcctg
gaggccctggatgtgcacacgtgcaaggcccccaagagtgccgactgggcgtctcccaca
tga
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