Felis catus (domestic cat): 101099392
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Entry
101099392 CDS
T02385
Symbol
WNT6
Name
(RefSeq) protein Wnt-6
KO
K00445
wingless-type MMTV integration site family, member 6
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
101099392 (WNT6)
04390 Hippo signaling pathway
101099392 (WNT6)
04150 mTOR signaling pathway
101099392 (WNT6)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
101099392 (WNT6)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
101099392 (WNT6)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
101099392 (WNT6)
05205 Proteoglycans in cancer
101099392 (WNT6)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
101099392 (WNT6)
05226 Gastric cancer
101099392 (WNT6)
05217 Basal cell carcinoma
101099392 (WNT6)
05224 Breast cancer
101099392 (WNT6)
09172 Infectious disease: viral
05165 Human papillomavirus infection
101099392 (WNT6)
09164 Neurodegenerative disease
05010 Alzheimer disease
101099392 (WNT6)
05022 Pathways of neurodegeneration - multiple diseases
101099392 (WNT6)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
101099392 (WNT6)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
fca00536
]
101099392 (WNT6)
Glycosaminoglycan binding proteins [BR:
fca00536
]
Heparan sulfate / Heparin
Morphogens
101099392 (WNT6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
101099392
NCBI-ProteinID:
XP_023115452
UniProt:
A0A337SM97
LinkDB
All DBs
Position
C1:202754424..202767993
Genome browser
AA seq
365 aa
AA seq
DB search
MLPPAPSLLGLLLLLLLCPAHVGGLWWAVGSPLVMDPTSICRKARRLAGRQAELCQAEPE
VVAELARGARLGVRECQFQFRFRRWNCSSHSKAFGRILQQDIRETAFVFAITAAGASHAV
TQACSMGELLQCGCQAPRGRAPPRPPGLPGTPGPPGPAGSPDGSAAWEWGGCGDDVDFGD
EKSRLFMDARHKRGRGDIRALVQLHNNEAGRLAVRSHTRTECKCHGLSGSCALRTCWQKL
PPFREVGARLLERFHGASRVMGTNDGKALLPAVRTLKPPGRADLLYAADSPDFCAPNRRT
GSPGTRGRACNSSALDLSGCDLLCCGRGHRQESVQLEENCLCRFHWCCVVQCHRCRVRKE
LSLCL
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctgccgcccgcgccctccctcctcgggctgctgctgctgctgctcctgtgtcccgcg
cacgtcggcggactgtggtgggcggtgggcagccccttggtcatggatcctaccagcatc
tgcaggaaagcgcggcggctggcagggcggcaggctgagttgtgccaggccgagccagag
gtggtggcggagctagcccggggcgcccggctcggggtgcgggagtgccagttccagttc
cgattccgccgctggaactgctccagccacagcaaggccttcgggcgcatcctgcagcag
gacatccgggagacggccttcgtgttcgctataacggccgcgggcgccagccacgccgtc
acgcaggcctgctccatgggcgagctgctgcagtgcggctgccaggcgccccgagggcgg
gccccgccgcgtcccccgggcctgcccggcacccctgggccccccggccccgccggctcc
cccgacggcagcgccgcctgggagtgggggggctgcggcgacgatgtggacttcggggac
gagaagtcgaggctctttatggacgcgcggcacaagcggggacgcggagacatccgtgcg
ttggtgcaactgcacaacaacgaggccggccggctggccgtacggagccacacgcgcacc
gagtgcaagtgccatgggctgtcgggctcgtgcgcgctgcgaacctgctggcagaagctg
cccccgttccgggaggtgggcgcgcggctgctcgagcgcttccacggcgcctcgcgtgtc
atgggaaccaacgacggcaaggctctgctgcccgcggtccgcactcttaagccgccgggc
cgcgccgacctgctctacgccgccgactcgcccgacttctgcgctcccaaccggcgcacc
ggctcgccgggcacgcgcggccgcgcctgcaacagcagtgccctggacctcagcggctgt
gacctgctgtgctgcggccgcgggcaccgccaggagagcgtgcagctcgaggagaactgc
ctgtgtcgcttccactggtgctgtgtggtgcagtgccaccgctgccgcgtgcgcaaggag
ctcagcctctgcctctga
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