Capra hircus (goat): 102169419
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Entry
102169419 CDS
T02910
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
KO
K01064
wingless-type MMTV integration site family, member 9
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
102169419 (WNT9B)
04390 Hippo signaling pathway
102169419 (WNT9B)
04150 mTOR signaling pathway
102169419 (WNT9B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102169419 (WNT9B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102169419 (WNT9B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102169419 (WNT9B)
05205 Proteoglycans in cancer
102169419 (WNT9B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102169419 (WNT9B)
05226 Gastric cancer
102169419 (WNT9B)
05217 Basal cell carcinoma
102169419 (WNT9B)
05224 Breast cancer
102169419 (WNT9B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102169419 (WNT9B)
09164 Neurodegenerative disease
05010 Alzheimer disease
102169419 (WNT9B)
05022 Pathways of neurodegeneration - multiple diseases
102169419 (WNT9B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102169419 (WNT9B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
chx00536
]
102169419 (WNT9B)
Glycosaminoglycan binding proteins [BR:
chx00536
]
Heparan sulfate / Heparin
Morphogens
102169419 (WNT9B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
102169419
NCBI-ProteinID:
XP_017919504
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All DBs
Position
19:complement(44964195..44986626)
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AA seq
561 aa
AA seq
DB search
MAAPIFPQAPSAFVFTKPSRPSFSVAELGQRGPHQPAWRVDETRLLRLQAPLSFCPFLRV
PPAGTFLRSPGPSTAQSPDKPYISPAGGWWLRCERCAARGDATGLRAAGIMRPPPALALA
ALCLLALPAAAAAAYFGPVRDLILPTKPDLGSRFKLWDSAGVSDLVPVRPSAPCPCRSKE
SLPRSDVLSDPHFPQEGPLPLTCPPSLGIVIFHLQSQPPRVTGLPSLAPFRLTGREVLTP
FPGLGTAAPAQGGAHLKQCDLLKLSRRQKQLCRREPGLAETLQDAAHLSLLECQFQFRHE
RWNCSLEGRTGLLKRGFKETAFLYAVSAAALTHTLARACSAGRMERCTCDDSPGLESRQA
WQWGVCGDNLKYSTKFLNNFLGPKRGSKDLRARTDAHNTHVGIKAVKSGLRTTCKCHGVS
GSCAVRTCWKQLSPFRETGQVLKLRYDSAVKVSSATNEALGRLELWAPARPGSPTQGPAP
RPGDLVYMEDSPSFCRPSKYSPGTGGRVCSREASCSSLCCGRGYDTQSRLAAFSCHCQVQ
WCCYVECQQCVREELVYTCKH
NT seq
1686 nt
NT seq
+upstream
nt +downstream
nt
atggcagctcccatcttcccccaggctcccagcgccttcgtgttcacaaagccaagccgg
ccctccttcagtgtcgcggagctggggcagaggggcccgcaccaaccggcttggagggtg
gatgagacacgacttctcagactccaggcgcctctctccttttgccccttcctgcgggta
cctcctgcgggtaccttcctgcggtccccgggtccttcaaccgcccagtcgcccgacaag
ccctacatcagccctgcgggcggctggtggctgcgctgcgagcgctgcgcggcgcgagga
gatgcaactgggctccgcgccgccggcatcatgcgccccccgcccgcgctggccctggcc
gcgctctgcctgctggcgctgcccgccgccgccgccgccgcctacttcggtcctgtccga
gacctcatcctgcccactaagccggatctcggatcccggttcaagctctgggactctgca
ggcgtctcggacctggtgcctgtgcgccccagcgcgccctgtccctgccggtccaaggag
tccctcccgcgctcggacgtcctctccgatcctcacttcccccaagaaggcccccttccc
ctcacatgtcccccatccttagggattgtcatctttcaccttcaatcacaaccccccagg
gtcactggtctcccttctcttgctccctttagactgaccgggcgggaggtcctgacgccc
ttccccgggctgggcactgctgccccagcacagggtggggcccacctgaagcagtgcgac
ctcctaaagttgtcccgccggcagaagcagctctgtcggcgggagccaggcttggctgag
accctgcaggacgccgcgcacctcagcctgctcgagtgccagtttcagttccggcatgag
cgctggaactgcagcctggaggggaggacggggctgctcaagagaggtttcaaggagacg
gccttcctgtatgcggtgtccgcggccgccctcacgcacactctggcccgggcctgcagc
gctggccgcatggagcggtgcacctgtgatgactccccgggcctcgagagccggcaagcc
tggcagtggggtgtgtgtggtgacaacctcaagtatagcaccaagttcctgaacaacttc
ctggggcccaagagaggaagcaaagatctgcgggcgcggacagacgcccacaacacccac
gtgggcatcaaggccgtgaagagtggcctccggaccacgtgtaagtgccatggcgtgtct
ggctcctgcgccgtgcgcacctgctggaagcagctgtccccgttccgcgagacaggccag
gtgctgaagctgcgctacgactcagccgtcaaggtgtccagtgccaccaatgaggccttg
ggccgcctggagctgtgggcaccggccagaccaggcagccccacccagggccccgcgccg
cggcccggggacctggtctacatggaggactcccccagtttctgccggcccagcaagtac
tcgcctggcacagggggcagggtgtgttcccgcgaggccagctgcagcagcctgtgctgc
gggcggggctacgacacccagagccgcctggcggccttctcctgccactgccaggtgcag
tggtgctgctacgtggagtgccagcagtgtgtgcgggaggagcttgtatacacctgtaag
cactag
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