Capra hircus (goat): 102171665
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Entry
102171665 CDS
T02910
Symbol
WNT7A
Name
(RefSeq) protein Wnt-7a
KO
K00572
wingless-type MMTV integration site family, member 7
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
102171665 (WNT7A)
04390 Hippo signaling pathway
102171665 (WNT7A)
04150 mTOR signaling pathway
102171665 (WNT7A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
102171665 (WNT7A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
102171665 (WNT7A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102171665 (WNT7A)
05205 Proteoglycans in cancer
102171665 (WNT7A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
102171665 (WNT7A)
05226 Gastric cancer
102171665 (WNT7A)
05217 Basal cell carcinoma
102171665 (WNT7A)
05224 Breast cancer
102171665 (WNT7A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
102171665 (WNT7A)
09164 Neurodegenerative disease
05010 Alzheimer disease
102171665 (WNT7A)
05022 Pathways of neurodegeneration - multiple diseases
102171665 (WNT7A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102171665 (WNT7A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
chx00536
]
102171665 (WNT7A)
Glycosaminoglycan binding proteins [BR:
chx00536
]
Heparan sulfate / Heparin
Morphogens
102171665 (WNT7A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
102171665
NCBI-ProteinID:
XP_017922161
UniProt:
A0A452FN72
LinkDB
All DBs
Position
22:58082523..58146522
Genome browser
AA seq
349 aa
AA seq
DB search
MNRKARRCLGHFFLSLGMVYLRIGGFSSVVALGASIICNKIPGLAPRQRAICQSRPDAII
VIGEGSQMGLDECQFQFRNGRWNCSALGERTVFGKELKVGSREAAFTYAIIAAGVAHAIT
AACTQGNLSDCGCDKEKQGQYHRDEGWKWGGCSADIRYGIGFAKVFVDAREIKQNARTLM
NLHNNEAGRKILEENMKLECKCHGVSGSCTTKTCWTTLPQFRELGYVLKDKYNEAVHVEP
VRASRNKRPTFLKIKKPLSYRKPMDTDLVYIEKSPNYCEEDPATGSVGTQGRACNKTAPQ
ASGCDLMCCGRGYNTHQYARAWQCSCRFHWCCYVKCNTCSERTEVYTCK
NT seq
1050 nt
NT seq
+upstream
nt +downstream
nt
atgaaccggaaagcgcggcgctgcctgggccacttctttctcagcctgggcatggtctac
ctccggatcggcggcttctcctcggtggtagctctgggcgcaagcatcatctgtaacaag
atcccaggcctggcccccagacagcgggcgatctgccagagccggcccgacgccatcatc
gtcataggagaaggctcgcaaatgggcctggacgagtgtcagtttcaattccgcaacggc
cgctggaactgctcggcactgggggagcgcaccgtcttcggcaaggagctcaaagtgggg
agccgggaggctgccttcacctacgccatcatcgccgcgggcgtggcccatgccatcaca
gcagcctgcacccagggcaacctgagcgactgcggctgcgacaaggagaagcagggccag
taccaccgggacgagggctggaagtggggtggctgctctgccgacatccgctatggcatc
ggcttcgccaaggtctttgtggacgcccgggagatcaagcagaacgcccggactctcatg
aacttacacaataacgaggcaggccggaagatcctggaggagaacatgaagctggagtgc
aagtgccacggcgtgtcgggctcctgcaccaccaagacctgctggaccacgctgccgcag
ttccgcgagctgggctacgtgctcaaggacaagtacaacgaggcagtccacgtggagccg
gtgcgcgccagccgcaacaagcggcccaccttcctcaagatcaagaagccgctgtcctac
cgcaagcccatggacaccgacctggtgtacatcgagaagtcgcccaactactgcgaggag
gacccggcgacgggcagcgtgggcacgcagggccgcgcctgcaacaagacggcgccccag
gccagcggctgcgacctcatgtgctgcggccgcggctacaacacccaccagtacgcccgc
gcgtggcagtgcagctgcaggttccactggtgctgctacgtcaagtgcaacacttgcagc
gagcgcaccgaggtctacacgtgcaagtga
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