Talpa occidentalis (Iberian mole): 119236432
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Entry
119236432 CDS
T07495
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
tod
Talpa occidentalis (Iberian mole)
Pathway
tod04150
mTOR signaling pathway
tod04310
Wnt signaling pathway
tod04390
Hippo signaling pathway
tod04550
Signaling pathways regulating pluripotency of stem cells
tod04916
Melanogenesis
tod04934
Cushing syndrome
tod05010
Alzheimer disease
tod05022
Pathways of neurodegeneration - multiple diseases
tod05165
Human papillomavirus infection
tod05200
Pathways in cancer
tod05205
Proteoglycans in cancer
tod05217
Basal cell carcinoma
tod05224
Breast cancer
tod05225
Hepatocellular carcinoma
tod05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
tod00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
119236432 (WNT2B)
04390 Hippo signaling pathway
119236432 (WNT2B)
04150 mTOR signaling pathway
119236432 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
119236432 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
119236432 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
119236432 (WNT2B)
05205 Proteoglycans in cancer
119236432 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
119236432 (WNT2B)
05226 Gastric cancer
119236432 (WNT2B)
05217 Basal cell carcinoma
119236432 (WNT2B)
05224 Breast cancer
119236432 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
119236432 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
119236432 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
119236432 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
119236432 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
tod00536
]
119236432 (WNT2B)
Glycosaminoglycan binding proteins [BR:
tod00536
]
Heparan sulfate / Heparin
Morphogens
119236432 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
119236432
NCBI-ProteinID:
XP_037356161
LinkDB
All DBs
Position
Unknown
AA seq
394 aa
AA seq
DB search
MRRPRAAGRAAQPPPRRARAPLRARAPRPAAPDGSRAPAGPRLARLLPLLLLLALPARVD
TSWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWN
CTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSACSCDPYSRGRHH
DQRGDFDWGGCSDNIRYGISFAKTFVDAKEKRLKDARALMNLHNNRCGRRAVRRFLKLEC
KCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGNRHATRD
DLVYFDNSPDYCALDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCEC
KFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1185 nt
NT seq
+upstream
nt +downstream
nt
atgcggaggccgcgcgccgcggggagagccgcgcagccgcccccccggcgcgcccgagcc
ccgctccgcgcgcgcgcgccccgacccgcggcccccgacggctcccgggccccggccggc
ccgcgcctcgcccgcctgctgccgctgctgctgctgctggcgctgcccgcccgcgtggac
acgtcctggtggtacatcggcgccctcggggcccgcgtgatctgtgacaacatccctggg
ctggtgagtcggcagcggcagctgtgccagcgctacccggacatcatgcgctcggtgggc
gaaggggcccgggagtggatccgggagtgtcagcaccagttccgccaccaccgctggaac
tgcaccacgctggaccgcgaccacaccgtcttcggccgcgtcatgctcagaagcagccgg
gaggcggcgttcgtgtacgccatctcgtccgcgggggtggtgcacgccatcacgcgcgcc
tgcagccagggtgagctgagcgcgtgcagctgtgacccctactcccgcggccgacaccac
gaccagcgtggggactttgactggggtggctgcagtgacaatatccgctatggcatttcg
tttgccaagaccttcgtggatgccaaggagaagaggcttaaagatgcccgggccctcatg
aacttacataacaaccgctgcggccgcagggctgtgcggcggtttctgaagctggagtgt
aagtgccacggcgtgagcggctcctgcacgctgcgcacctgctggcgcgccctctcggac
ttccgccgcacgggggactacctgcggcggcgctacgacggggccgtgcaggtgacggcc
acccaggacggcgccaacttcacagcagcgcgccagggcaaccgccacgccacccgggat
gaccttgtctacttcgacaactccccggactactgcgccttggacaaggcggcaggttcc
ctaggcaccgcgggccgggtctgcagcaagacatcgaaagggacagacggctgtgaaatc
atgtgctgtggccgagggtatgacacaactcgagtcacccgtgtcacccagtgtgagtgc
aaattccactggtgctgtgccgtgcgctgcaaggagtgcagaaacactgtggatgtccac
acgtgcaaggcccccaagaaggcagagtggctggaccagacctga
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