Phascolarctos cinereus (koala): 110201658
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Entry
110201658 CDS
T05867
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b
KO
K00572
wingless-type MMTV integration site family, member 7
Organism
pcw
Phascolarctos cinereus (koala)
Pathway
pcw04150
mTOR signaling pathway
pcw04310
Wnt signaling pathway
pcw04390
Hippo signaling pathway
pcw04550
Signaling pathways regulating pluripotency of stem cells
pcw04916
Melanogenesis
pcw04934
Cushing syndrome
pcw05010
Alzheimer disease
pcw05022
Pathways of neurodegeneration - multiple diseases
pcw05165
Human papillomavirus infection
pcw05200
Pathways in cancer
pcw05205
Proteoglycans in cancer
pcw05217
Basal cell carcinoma
pcw05224
Breast cancer
pcw05225
Hepatocellular carcinoma
pcw05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pcw00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
110201658 (WNT7B)
04390 Hippo signaling pathway
110201658 (WNT7B)
04150 mTOR signaling pathway
110201658 (WNT7B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
110201658 (WNT7B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
110201658 (WNT7B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
110201658 (WNT7B)
05205 Proteoglycans in cancer
110201658 (WNT7B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
110201658 (WNT7B)
05226 Gastric cancer
110201658 (WNT7B)
05217 Basal cell carcinoma
110201658 (WNT7B)
05224 Breast cancer
110201658 (WNT7B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
110201658 (WNT7B)
09164 Neurodegenerative disease
05010 Alzheimer disease
110201658 (WNT7B)
05022 Pathways of neurodegeneration - multiple diseases
110201658 (WNT7B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
110201658 (WNT7B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pcw00536
]
110201658 (WNT7B)
Glycosaminoglycan binding proteins [BR:
pcw00536
]
Heparan sulfate / Heparin
Morphogens
110201658 (WNT7B)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
110201658
NCBI-ProteinID:
XP_020833143
UniProt:
A0A6P5JIB6
LinkDB
All DBs
Position
Unknown
AA seq
349 aa
AA seq
DB search
MHRNFRKWIFYVFLCFGVLYVKLGALSSVVALGANIICNKIPGLAPRQRAICQSRPDAII
VIGEGAQMGINECQYQFRYGRWNCSALGEKTVFGQELRVGSREAAFTYAITAAGVAHAVT
AACSQGNLSNCGCDREKQGYYNQEEGWKWGGCSADVRYGIEFSRRFVDAREIKKNARRLM
NLHNNEAGRKVLEERMKLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYNAAVQVEV
VRASRLRQPTFLKVKQLRSYQKPLDTDLVYIEKSPNYCEEDAATGSVGTQGRLCNRTSPG
ADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq
1050 nt
NT seq
+upstream
nt +downstream
nt
atgcacagaaactttcgcaagtggattttctacgtgtttctctgctttggcgtcctctac
gtgaagctgggagctctgtcatctgtggtggctttgggagccaatatcatctgcaacaag
atccctggcctggccccccgacaacgagccatctgtcagagccgccccgacgccatcatc
gtgattggagaaggggcacagatggggatcaacgaatgtcaataccagttccgctatggc
cgatggaactgttctgcacttggcgagaagaccgtctttgggcaggaacttcgagtgggg
agtcgggaagctgccttcacttatgcaatcacagctgctggagtggcccacgcggtcacc
gcggcctgcagccagggcaacctaagcaactgcggctgtgacagggagaagcaaggctac
tacaaccaggaggagggctggaagtggggcggctgctcggccgatgtccgctacggcatc
gagttctccaggcgcttcgttgatgcccgcgagatcaagaagaacgccaggcgcctgatg
aacctgcataacaacgaggccggaagaaaggtgctcgaggaaaggatgaagctcgaatgc
aaatgccacggggtgtcgggctcgtgcaccaccaagacgtgctggaccacgctgcccaag
ttccgggaggtcggccacctgctcaaggagaagtacaacgcggccgtgcaggtggaggtg
gtgcgcgccagccggctgcgccagcccaccttcctcaaggtcaagcagctgcgcagctac
cagaagcccctggacacggacctggtctacatcgagaagtcccccaactactgcgaggag
gacgccgccacgggcagcgtgggcactcagggccgactgtgtaaccgcacgtcgcccggc
gccgacggctgcgacaccatgtgctgcggccggggctacaacacgcaccagtacaccaag
gtctggcagtgcaactgcaaatttcactggtgctgtttcgtcaaatgcaacacgtgcagc
gagcggactgaggtgttcacctgcaagtag
DBGET
integrated database retrieval system