Sus scrofa (pig): 100626947
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Entry
100626947 CDS
T01009
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
KO
K00572
wingless-type MMTV integration site family, member 7
Organism
ssc
Sus scrofa (pig)
Pathway
ssc04150
mTOR signaling pathway
ssc04310
Wnt signaling pathway
ssc04390
Hippo signaling pathway
ssc04550
Signaling pathways regulating pluripotency of stem cells
ssc04916
Melanogenesis
ssc04934
Cushing syndrome
ssc05010
Alzheimer disease
ssc05022
Pathways of neurodegeneration - multiple diseases
ssc05165
Human papillomavirus infection
ssc05200
Pathways in cancer
ssc05205
Proteoglycans in cancer
ssc05217
Basal cell carcinoma
ssc05224
Breast cancer
ssc05225
Hepatocellular carcinoma
ssc05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ssc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100626947 (WNT7B)
04390 Hippo signaling pathway
100626947 (WNT7B)
04150 mTOR signaling pathway
100626947 (WNT7B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100626947 (WNT7B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100626947 (WNT7B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100626947 (WNT7B)
05205 Proteoglycans in cancer
100626947 (WNT7B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100626947 (WNT7B)
05226 Gastric cancer
100626947 (WNT7B)
05217 Basal cell carcinoma
100626947 (WNT7B)
05224 Breast cancer
100626947 (WNT7B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100626947 (WNT7B)
09164 Neurodegenerative disease
05010 Alzheimer disease
100626947 (WNT7B)
05022 Pathways of neurodegeneration - multiple diseases
100626947 (WNT7B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100626947 (WNT7B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ssc00536
]
100626947 (WNT7B)
Glycosaminoglycan binding proteins [BR:
ssc00536
]
Heparan sulfate / Heparin
Morphogens
100626947 (WNT7B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
100626947
NCBI-ProteinID:
XP_020947043
UniProt:
A0A4X1W4X7
LinkDB
All DBs
Position
5:3521412..3572322
Genome browser
AA seq
349 aa
AA seq
DB search
MHRNFRKWIFYVFLCFGVLYVKLGALSSVVALGANIICNKIPGLAPRQRAICQSRPDAII
VIGEGAQMGINECQYQFRFGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHAVT
AACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIKKNARRLM
NLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNVAVQVEV
VRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPG
ADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq
1050 nt
NT seq
+upstream
nt +downstream
nt
atgcacagaaactttcgcaagtggattttctacgtgtttctctgctttggcgttctctac
gtgaagcttggagcgctgtcatccgtcgtggccctgggagccaacatcatttgcaacaag
atccctggcttggccccgcggcagcgcgccatctgccagagccggcccgatgccatcatc
gtgatcggggagggggcacagatgggcatcaacgagtgccagtaccagttccgcttcgga
cgctggaactgctccgccctcggcgagaagacggtcttcgggcaagagctccgagtaggg
agccgtgaggccgccttcacgtatgccatcaccgccgccggcgtggcccacgctgtcacc
gccgcctgcagccagggcaacctgagcaactgcgggtgcgaccgcgagaagcagggttac
tacaaccaggccgagggctggaagtggggcggctgctccgccgacgtgcgctacggcatc
gacttctcccggcgcttcgtggacgcccgcgagatcaagaaaaacgcccggcgcctcatg
aacctgcacaacaacgaggcgggcaggaaggtcctggaggagcgcatgaagctggagtgc
aagtgccacggcgtgtcgggctcgtgcaccaccaagacgtgctggaccacgctgcccaag
ttccgcgaggtgggccacttgctcaaggagaagtacaacgtggcggtgcaggtggaggta
gtgcgcgccagccgcctgcggcagcccaccttcctgcgcatcaagcagctgcgcagctac
cagaagcccatggagacggacctggtgtacatcgagaagtcgcccaactactgcgaggag
gacgcggccacgggcagcgtgggcacgcagggccgcctgtgcaaccgcacctcgcccggg
gctgacggctgcgacaccatgtgctgcggccgcgggtacaacacccaccagtacaccaag
gtctggcagtgcaactgcaagttccactggtgctgcttcgtcaagtgcaacacgtgcagc
gagcgcactgaggtcttcacctgcaagtga
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