Neogale vison (American mink): 122900330
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Entry
122900330 CDS
T08764
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
nvs
Neogale vison (American mink)
Pathway
nvs04150
mTOR signaling pathway
nvs04310
Wnt signaling pathway
nvs04390
Hippo signaling pathway
nvs04550
Signaling pathways regulating pluripotency of stem cells
nvs04916
Melanogenesis
nvs04934
Cushing syndrome
nvs05010
Alzheimer disease
nvs05022
Pathways of neurodegeneration - multiple diseases
nvs05165
Human papillomavirus infection
nvs05200
Pathways in cancer
nvs05205
Proteoglycans in cancer
nvs05217
Basal cell carcinoma
nvs05224
Breast cancer
nvs05225
Hepatocellular carcinoma
nvs05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
nvs00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
122900330 (WNT2B)
04390 Hippo signaling pathway
122900330 (WNT2B)
04150 mTOR signaling pathway
122900330 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
122900330 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
122900330 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
122900330 (WNT2B)
05205 Proteoglycans in cancer
122900330 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
122900330 (WNT2B)
05226 Gastric cancer
122900330 (WNT2B)
05217 Basal cell carcinoma
122900330 (WNT2B)
05224 Breast cancer
122900330 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
122900330 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
122900330 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
122900330 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
122900330 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
nvs00536
]
122900330 (WNT2B)
Glycosaminoglycan binding proteins [BR:
nvs00536
]
Heparan sulfate / Heparin
Morphogens
122900330 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
122900330
NCBI-ProteinID:
XP_044094858
UniProt:
A0A8C7A2A3
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All DBs
Position
2:96928913..96941202
Genome browser
AA seq
393 aa
AA seq
DB search
MVKPDSAEEAAQLPPRRTRAPVPALGPGPAAPDGSRASARLGLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDIHTCKAPKKAEWLDQT
NT seq
1182 nt
NT seq
+upstream
nt +downstream
nt
atggtgaagccggatagtgcggaggaagccgcgcagctcccgcctcggcgcacccgtgcc
cctgtccccgcgctcgggccaggacccgcggcccccgacggctctcgggcttctgcccgc
ctcggtcttgcctgcctgctactgctgttgctgctgacgctcccggcccgcgtagacaca
tcctggtggtacatcggggccctgggggcccgagtgatctgtgacaatattcctggtctg
gtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctcagtgggcgag
ggtgcccgagaatggatccgagagtgccagcaccagttccgccaccaccgctggaactgc
accacgctggacagggaccacactgtctttggccgtgtcatgctcagaagcagccgagag
gcagcatttgtatacgccatctcgtcagcaggggtggtccatgctattacccgcgcctgt
agccagggtgaactgagtgtgtgcagctgtgacccctacactcgtggccgacaccatgac
caacgtggagattttgactggggtggctgcagtgacaacatccactatggtgttcgcttt
gccaaggcctttgtggatgccaaggaaaagaggctcaaggatgcccgggccctcatgaac
ttacataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctcgagtgtaag
tgccacggcgtaagcggctcctgtactctgcgaacctgctggcgtgcgctctcagacttc
cgccgcacaggtgactacctgcggcggcgctatgacggcgctgtgcaggtgacagcaacc
caggatggcgccaacttcacagcagcccgccaaggctatcgccgtgccacccggactgac
cttgtctacttcgacaactccccagactactgtgtcttggacaaggctgccggttcccta
ggcaccgcgggccgtgtctgcagcaagacatctaaagggacagatggttgcgaaatcatg
tgctgtggccgagggtatgacacaactcgagtcacccgcgtcacccagtgtgagtgcaag
ttccactggtgctgtgcagtgcggtgtaaggagtgcagaaacactgtggacatccacacg
tgcaaggcccccaagaaggcagagtggctggaccagacctga
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