Oryctolagus cuniculus (rabbit): 100126569
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Entry
100126569 CDS
T03373
Symbol
WNT2
Name
(RefSeq) protein Wnt-2 precursor
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
ocu
Oryctolagus cuniculus (rabbit)
Pathway
ocu04150
mTOR signaling pathway
ocu04310
Wnt signaling pathway
ocu04390
Hippo signaling pathway
ocu04550
Signaling pathways regulating pluripotency of stem cells
ocu04916
Melanogenesis
ocu04934
Cushing syndrome
ocu05010
Alzheimer disease
ocu05022
Pathways of neurodegeneration - multiple diseases
ocu05165
Human papillomavirus infection
ocu05200
Pathways in cancer
ocu05205
Proteoglycans in cancer
ocu05217
Basal cell carcinoma
ocu05224
Breast cancer
ocu05225
Hepatocellular carcinoma
ocu05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ocu00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100126569 (WNT2)
04390 Hippo signaling pathway
100126569 (WNT2)
04150 mTOR signaling pathway
100126569 (WNT2)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100126569 (WNT2)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100126569 (WNT2)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100126569 (WNT2)
05205 Proteoglycans in cancer
100126569 (WNT2)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100126569 (WNT2)
05226 Gastric cancer
100126569 (WNT2)
05217 Basal cell carcinoma
100126569 (WNT2)
05224 Breast cancer
100126569 (WNT2)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100126569 (WNT2)
09164 Neurodegenerative disease
05010 Alzheimer disease
100126569 (WNT2)
05022 Pathways of neurodegeneration - multiple diseases
100126569 (WNT2)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100126569 (WNT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ocu00536
]
100126569 (WNT2)
Glycosaminoglycan binding proteins [BR:
ocu00536
]
Heparan sulfate / Heparin
Morphogens
100126569 (WNT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100126569
NCBI-ProteinID:
NP_001164513
Ensembl:
ENSOCUG00000016173
UniProt:
Q09YN1
LinkDB
All DBs
Position
7:complement(145617271..145661302)
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AA seq
360 aa
AA seq
DB search
MNAPLGGIWLGLPLLLTWLSPEVSSSWWYMRATGDSSRVMCDNVPGLVSRQRQLCHRHPD
VMRAIGLGVAEWTAECQYQFRQHRWNCNTLDRDHGLFGRVLLRSSRESAFVYAISSAGVV
FAITRACSQGELKSCSCDPKKKGTAKDSKGTFDWGGCSDNIDYGIKFARAFVDAKERKGK
DARALMNLHNNRAGRKAVKRFLKQECKCHGVSGSCTLRTCWLAMADFRKTGDYLWRKYNG
AIQVVMNQDGTGFTVANKRFKKPTKNDLVYFENSPDYCIRDREAGSPGTAGRVCNLTSRG
MDSCEVMCCGRGYDTSRVTRMTKCECKFHWCCAVRCQDCLEALDVHTCKAPKSADWTTPT
NT seq
1083 nt
NT seq
+upstream
nt +downstream
nt
atgaacgcccctctcggtggaatctggctggggctccctctgctcttgacctggctcagc
cccgaggtcagctcttcatggtggtacatgagagctacaggtgactcctccagggtgatg
tgtgacaatgtgccaggcctggtgagccgccagcggcagctgtgccaccgacacccggac
gtgatgcgtgccataggcctgggtgtggccgagtggacagcagagtgccagtatcagttc
cgacagcaccgctggaactgcaacaccctggacagggatcacggcctctttggcagggtt
ctgctccgaagtagtcgggaatctgcctttgtatacgccatctcctcagctggagttgta
tttgccatcaccagggcctgtagccaaggagaattaaaatcctgttcctgtgatccaaag
aagaaaggaactgccaaggacagcaagggcaccttcgactggggtggctgcagtgataac
attgactatgggatcaagtttgcccgagcctttgtggatgccaaggaaaggaaaggaaag
gatgccagagcgctgatgaatcttcacaacaacagagcgggcaggaaggctgtaaagcgg
ttcttgaaacaagagtgcaagtgccacggtgtgagcggctcgtgtactctgcggacgtgc
tggctggccatggccgacttcaggaaaacgggcgattacctctggaggaagtacaatgga
gccatccaggtcgtcatgaaccaggatggcactggtttcactgtggctaacaagaggttt
aagaagccaacgaaaaatgaccttgtgtactttgagaattctccagactactgtatcagg
gaccgagaggcaggctccccgggtacagcaggtcgtgtgtgcaacctgacgtccagaggc
atggacagctgtgaagtcatgtgctgcgggagaggctacgacacctcccgcgtcacccgg
atgaccaagtgcgagtgtaagttccactggtgctgtgccgtgcgttgccaggactgcctg
gaggccctggacgtgcacacatgcaaggctcccaagagtgctgactggacaaccccaaca
tga
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