Felis catus (domestic cat): 101080844
Help
Entry
101080844 CDS
T02385
Symbol
WNT9B
Name
(RefSeq) protein Wnt-9b
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
fca
Felis catus (domestic cat)
Pathway
fca04150
mTOR signaling pathway
fca04310
Wnt signaling pathway
fca04390
Hippo signaling pathway
fca04550
Signaling pathways regulating pluripotency of stem cells
fca04916
Melanogenesis
fca04934
Cushing syndrome
fca05010
Alzheimer disease
fca05022
Pathways of neurodegeneration - multiple diseases
fca05165
Human papillomavirus infection
fca05200
Pathways in cancer
fca05205
Proteoglycans in cancer
fca05217
Basal cell carcinoma
fca05224
Breast cancer
fca05225
Hepatocellular carcinoma
fca05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
fca00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
101080844 (WNT9B)
04390 Hippo signaling pathway
101080844 (WNT9B)
04150 mTOR signaling pathway
101080844 (WNT9B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
101080844 (WNT9B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
101080844 (WNT9B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101080844 (WNT9B)
05205 Proteoglycans in cancer
101080844 (WNT9B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
101080844 (WNT9B)
05226 Gastric cancer
101080844 (WNT9B)
05217 Basal cell carcinoma
101080844 (WNT9B)
05224 Breast cancer
101080844 (WNT9B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
101080844 (WNT9B)
09164 Neurodegenerative disease
05010 Alzheimer disease
101080844 (WNT9B)
05022 Pathways of neurodegeneration - multiple diseases
101080844 (WNT9B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
101080844 (WNT9B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
fca00536
]
101080844 (WNT9B)
Glycosaminoglycan binding proteins [BR:
fca00536
]
Heparan sulfate / Heparin
Morphogens
101080844 (WNT9B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
101080844
NCBI-ProteinID:
XP_044900675
LinkDB
All DBs
Position
E1:complement(43991128..44016510)
Genome browser
AA seq
357 aa
AA seq
DB search
MRPPPALALAALCLLALPAAAAAYFGLTGREVLTPFPGLGTAAAPAQSGAHLKPCDLLKL
SRRQKQLCRREPGLAETLQDAAHLSLLECQFQFRHERWNCSLEGRTGLLKRGFKETAFLY
AMSSAALTHTLARACSAGRMERCTCDDSPGLESRQAWQWGVCGDNLKYSTKFLSNFLGPK
RGSKDLRARADAHNTHVGIKAVKSGLRTTCKCHGVSGSCAVRTCWKQLAPFRETGQALKL
RYDSAVKVSSATNEALGRLELWAPARPGSPTKGPAPRPGDLVYMEDSPSFCRPSKYSPGT
AGRVCSREASCSSLCCGRGYDTQSRLVAFSCHCQVQWCCYVECQQCVQEELMYTCKH
NT seq
1074 nt
NT seq
+upstream
nt +downstream
nt
atgcgccccccgcccgcgctggccctggccgcgctctgcctgctggcgctgcccgccgcc
gccgccgcctacttcggcctgaccgggcgggaggtcctgacacccttcccagggctgggc
accgctgcggccccagcacagagcggggcccacctgaagccgtgtgacctgctgaagctg
tcccgccgacagaaacagctctgccggagggagcccggcctggccgagaccctgcaggac
gctgctcacctcagcctgctcgagtgccagtttcagttccgacatgagcgctggaactgc
agtctggaggggaggacaggcctgctcaagagaggtttcaaggagacggccttcctgtat
gcaatgtcctccgctgccctcacccacactctggcccgggcctgcagcgccgggcgcatg
gagcgctgcacctgtgatgattctccgggcctggagagccggcaggcctggcagtggggc
gtgtgcggcgacaacctcaagtacagcaccaagttcctgagcaacttcctggggcccaag
agaggaagcaaagacctgagggcacgggcggacgctcacaacacccacgtgggcatcaag
gcagtgaagagtggcctcaggaccacatgtaagtgccacggtgtgtcgggctcctgtgcc
gtgcgcacctgctggaagcagctcgccccgttccgcgagacgggccaggcgctaaaactg
cgttatgactcagctgtcaaggtgtccagtgccaccaacgaggccttgggccgcctggag
ctgtgggcgcccgcccggccaggcagccccaccaagggcccggccccacggcccggggac
ctggtctatatggaagactcgcccagtttctgccggcccagcaagtactcgcccggcacg
gcgggcagggtgtgctcccgggaggccagctgcagcagcctgtgctgcgggcggggctat
gacacccagagccgcctggtggccttctcctgccactgccaggtgcagtggtgctgctac
gtggagtgccagcagtgtgtgcaggaggagctcatgtacacctgcaagcattag
DBGET
integrated database retrieval system