Puma concolor (puma): 112858017
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Entry
112858017 CDS
T08890
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
KO
K00572
wingless-type MMTV integration site family, member 7
Organism
pcoo
Puma concolor (puma)
Pathway
pcoo04150
mTOR signaling pathway
pcoo04310
Wnt signaling pathway
pcoo04390
Hippo signaling pathway
pcoo04550
Signaling pathways regulating pluripotency of stem cells
pcoo04916
Melanogenesis
pcoo04934
Cushing syndrome
pcoo05010
Alzheimer disease
pcoo05022
Pathways of neurodegeneration - multiple diseases
pcoo05165
Human papillomavirus infection
pcoo05200
Pathways in cancer
pcoo05205
Proteoglycans in cancer
pcoo05217
Basal cell carcinoma
pcoo05224
Breast cancer
pcoo05225
Hepatocellular carcinoma
pcoo05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pcoo00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
112858017 (WNT7A)
04390 Hippo signaling pathway
112858017 (WNT7A)
04150 mTOR signaling pathway
112858017 (WNT7A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
112858017 (WNT7A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
112858017 (WNT7A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
112858017 (WNT7A)
05205 Proteoglycans in cancer
112858017 (WNT7A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
112858017 (WNT7A)
05226 Gastric cancer
112858017 (WNT7A)
05217 Basal cell carcinoma
112858017 (WNT7A)
05224 Breast cancer
112858017 (WNT7A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
112858017 (WNT7A)
09164 Neurodegenerative disease
05010 Alzheimer disease
112858017 (WNT7A)
05022 Pathways of neurodegeneration - multiple diseases
112858017 (WNT7A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
112858017 (WNT7A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pcoo00536
]
112858017 (WNT7A)
Glycosaminoglycan binding proteins [BR:
pcoo00536
]
Heparan sulfate / Heparin
Morphogens
112858017 (WNT7A)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
112858017
NCBI-ProteinID:
XP_025777124
UniProt:
A0A6P6HMV9
LinkDB
All DBs
Position
Unknown
AA seq
217 aa
AA seq
DB search
MNRKARRCLGHLFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKGSALSLIRLDSVVDLLLVRIWVLVRAR
NT seq
654 nt
NT seq
+upstream
nt +downstream
nt
atgaaccggaaagcgcggcgctgcctgggccacctctttctcagcctgggcatggtctac
ctccggatcggtggcttctcctcggtggtagctctgggcgcgagcatcatctgtaacaag
atcccaggcctggctcccagacagcgggcgatctgccagagccgtcccgacgccatcatc
gtcataggagaaggctcacaaatgggcctggacgagtgtcagtttcagttccgcaatggc
cgctggaactgctctgcactgggagagcgcaccgtcttcgggaaggagctcaaagtgggg
agccgggaggctgccttcacgtacgccatcattgccgccggtgtggcccacgccatcaca
gctgcctgtacccaaggcaacctgagtgactgtggctgcgacaaggagaagcaaggccag
taccaccgggacgagggctggaagtggggtggctgttctgccgacatccgctacggcatc
ggcttcgccaaggtctttgtggatgcccgggagatcaagcagaatgcccggactctcatg
aacttacacaataacgaggcgggccgaaagggctctgccctcagcctcattcggctggac
tctgtcgtcgatttgctgctggtcaggatctgggtgctggtcagggcccggtga
DBGET
integrated database retrieval system