Capra hircus (goat): 102182009
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Entry
102182009 CDS
T02910
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b
KO
K00182
wingless-type MMTV integration site family, member 2
Organism
chx
Capra hircus (goat)
Pathway
chx04150
mTOR signaling pathway
chx04310
Wnt signaling pathway
chx04390
Hippo signaling pathway
chx04550
Signaling pathways regulating pluripotency of stem cells
chx04916
Melanogenesis
chx04934
Cushing syndrome
chx05010
Alzheimer disease
chx05022
Pathways of neurodegeneration - multiple diseases
chx05165
Human papillomavirus infection
chx05200
Pathways in cancer
chx05205
Proteoglycans in cancer
chx05217
Basal cell carcinoma
chx05224
Breast cancer
chx05225
Hepatocellular carcinoma
chx05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
chx00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
102182009 (WNT2B)
04390 Hippo signaling pathway
102182009 (WNT2B)
04150 mTOR signaling pathway
102182009 (WNT2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102182009 (WNT2B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102182009 (WNT2B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102182009 (WNT2B)
05205 Proteoglycans in cancer
102182009 (WNT2B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102182009 (WNT2B)
05226 Gastric cancer
102182009 (WNT2B)
05217 Basal cell carcinoma
102182009 (WNT2B)
05224 Breast cancer
102182009 (WNT2B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102182009 (WNT2B)
09164 Neurodegenerative disease
05010 Alzheimer disease
102182009 (WNT2B)
05022 Pathways of neurodegeneration - multiple diseases
102182009 (WNT2B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102182009 (WNT2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
chx00536
]
102182009 (WNT2B)
Glycosaminoglycan binding proteins [BR:
chx00536
]
Heparan sulfate / Heparin
Morphogens
102182009 (WNT2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
102182009
NCBI-ProteinID:
XP_013817993
UniProt:
A0A452DYJ8
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Position
3:89792693..89807801
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AA seq
394 aa
AA seq
DB search
MLRPGGAEESAQLPPRRVRSPVRESAARPTAPDGSRASARLSLACLLLLLLLLTLPARVD
TSWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWN
CTTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHH
DQRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLEC
KCHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRT
DLVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCEC
KFHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq
1185 nt
NT seq
+upstream
nt +downstream
nt
atgctgaggccgggtggtgcggaggaatccgcgcagctaccccctcgacgcgttcgctcc
cctgtccgcgagtcggctgccagacccacggcccccgacggctctcgggcttcggcccgc
ctaagtcttgcctgccttctgttgctgctactgctgctgacgctgccggcccgcgtagac
acgtcctggtggtacattggggcactaggggcccgtgtgatctgtgacaatatcccgggg
ctggtgagccggcagcggcagctgtgccagcgttacccagacatcatgcgctccgtgggc
gagggtgcccgagagtggatccgagagtgtcagcaccagttccgccaccatcgctggaac
tgcaccaccctggaccgggaccacactgtctttggccgtgtcatgctcagaagtagccgg
gaggcagcatttgtatatgccatctcatcagcaggggtggtccatgctatcactcgtgcc
tgtagccagggtgaactgagtgtgtgcagctgtgacccctatacccgtggccgacaccat
gaccaacgtggggactttgactggggtggctgcagtgacaacatccactatggtgttcgc
tttgccaaagccttcgtggatgccaaggagaagaggcttaaggatgcccgggctctcatg
aacttacataacaatcgctgtggtcgcacggctgtgcggcggtttctgaagctggagtgt
aaatgccatggcgtgagtggctcctgtactctgcgcacctgctggcgagcgctctcagat
ttccgccgcacaggtgattacctgcggcggcgctatgacggggctgtgcaagtaacagcc
acccaggatggcgcaaacttcacggcagctcgccaaggctatcgccgtgctacccggact
gacctggtctactttgacaactccccagactactgtgtcttggacaaggctgcaggttcc
ctaggcactgcaggccgagtctgtagcaagacatctaaagggacagacggttgtgaaatc
atgtgctgcggccgagggtatgacacaactcgagttacccgtgtcacccagtgtgagtgc
aaattccactggtgctgtgctgtgcggtgcaaggagtgcagaaacactgtggacgtccat
acttgcaaggcccccaagaaggcagagtggctggatcagacctga
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