Equus asinus (ass): 106829346
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Entry
106829346 CDS
T04645
Symbol
WNT2
Name
(RefSeq) protein Wnt-2
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
eai
Equus asinus (ass)
Pathway
eai04150
mTOR signaling pathway
eai04310
Wnt signaling pathway
eai04390
Hippo signaling pathway
eai04550
Signaling pathways regulating pluripotency of stem cells
eai04916
Melanogenesis
eai04934
Cushing syndrome
eai05010
Alzheimer disease
eai05022
Pathways of neurodegeneration - multiple diseases
eai05165
Human papillomavirus infection
eai05200
Pathways in cancer
eai05205
Proteoglycans in cancer
eai05217
Basal cell carcinoma
eai05224
Breast cancer
eai05225
Hepatocellular carcinoma
eai05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
eai00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
106829346 (WNT2)
04390 Hippo signaling pathway
106829346 (WNT2)
04150 mTOR signaling pathway
106829346 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
106829346 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
106829346 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
106829346 (WNT2)
05205 Proteoglycans in cancer
106829346 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
106829346 (WNT2)
05226 Gastric cancer
106829346 (WNT2)
05217 Basal cell carcinoma
106829346 (WNT2)
05224 Breast cancer
106829346 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
106829346 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
106829346 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
106829346 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
106829346 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
eai00536
]
106829346 (WNT2)
Glycosaminoglycan binding proteins [BR:
eai00536
]
Heparan sulfate / Heparin
Morphogens
106829346 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
106829346
NCBI-ProteinID:
XP_014693894
UniProt:
A0A8C4LQ79
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All DBs
Position
1:27722827..27768812
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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
gaccgggatgcaggctccctgggtacagcaggccgcgtgtgcaacctgacttcccgaggg
atggacagctgtgaagtcatgtgctgcgggagaggctacgacacctcccgtgtcacccgg
atgaccaagtgtgagtgtaagttccattggtgctgtgccgtgcgctgtcaggactgcctg
gaggccctggatgtgcacacatgcaaggcccccaagagtgccgactgggcatctcccaca
tga
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