Pan troglodytes (chimpanzee): 104003805
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Entry
104003805 CDS
T01005
Symbol
WNT7B
Name
(RefSeq) protein Wnt-7b isoform X1
KO
K00572
wingless-type MMTV integration site family, member 7
Organism
ptr
Pan troglodytes (chimpanzee)
Pathway
ptr04150
mTOR signaling pathway
ptr04310
Wnt signaling pathway
ptr04390
Hippo signaling pathway
ptr04550
Signaling pathways regulating pluripotency of stem cells
ptr04916
Melanogenesis
ptr04934
Cushing syndrome
ptr05010
Alzheimer disease
ptr05022
Pathways of neurodegeneration - multiple diseases
ptr05165
Human papillomavirus infection
ptr05200
Pathways in cancer
ptr05205
Proteoglycans in cancer
ptr05217
Basal cell carcinoma
ptr05224
Breast cancer
ptr05225
Hepatocellular carcinoma
ptr05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
ptr00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
104003805 (WNT7B)
04390 Hippo signaling pathway
104003805 (WNT7B)
04150 mTOR signaling pathway
104003805 (WNT7B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
104003805 (WNT7B)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
104003805 (WNT7B)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
104003805 (WNT7B)
05205 Proteoglycans in cancer
104003805 (WNT7B)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
104003805 (WNT7B)
05226 Gastric cancer
104003805 (WNT7B)
05217 Basal cell carcinoma
104003805 (WNT7B)
05224 Breast cancer
104003805 (WNT7B)
09172 Infectious disease: viral
05165 Human papillomavirus infection
104003805 (WNT7B)
09164 Neurodegenerative disease
05010 Alzheimer disease
104003805 (WNT7B)
05022 Pathways of neurodegeneration - multiple diseases
104003805 (WNT7B)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
104003805 (WNT7B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
ptr00536
]
104003805 (WNT7B)
Glycosaminoglycan binding proteins [BR:
ptr00536
]
Heparan sulfate / Heparin
Morphogens
104003805 (WNT7B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
DUF6973
Motif
Other DBs
NCBI-GeneID:
104003805
NCBI-ProteinID:
XP_016794879
Ensembl:
ENSPTRG00000042983
VGNC:
12944
LinkDB
All DBs
Position
23:complement(47919141..47974092)
Genome browser
AA seq
356 aa
AA seq
DB search
MAQPPSLDHAQKLSQVDFLRVSLLWRPVREARSTVIRGGPGSQHHLQQDSWPSPTAACHL
PEPARCHHCDWGGGADGHQRVPVPVPLRTLELLCPRREDRLRARAPRSREAAFTYAITAA
GVAHAVTAACSQGNLSNCGCDREKQGYYNQAEGWKWGGCSADVRYGIDFSRRFVDAREIK
KNARRLMNLHNNEAGRKVLEDRMQLECKCHGVSGSCTTKTCWTTLPKFREVGHLLKEKYN
AAVQVEVVRASRLRQPTFLRIKQLRSYQKPMETDLVYIEKSPNYCEEDAATGSVGTQGRL
CNRTSPGADGCDTMCCGRGYNTHQYTKVWQCNCKFHWCCFVKCNTCSERTEVFTCK
NT seq
1071 nt
NT seq
+upstream
nt +downstream
nt
atggcgcagcccccctccctggatcatgcacagaaactttcgcaagtggattttctacgt
gtttctctgctttggcgtcctgtacgtgaagctcggagcactgtcatccgtggtggccct
gggagccaacatcatctgcaacaagattcctggcctagccccacggcagcgtgccatctg
ccagagccggcccgatgccatcattgtgattggggagggggcgcagatgggcatcaacga
gtgccagtaccagttccgcttcggacgctggaactgctctgccctcggcgagaagaccgt
cttcgggcaagagctccgaggagccgtgaggctgccttcacgtacgccatcaccgcggct
ggcgtagcgcacgccgtcaccgctgcctgcagccaaggcaacctgagcaactgcggctgc
gaccgcgagaagcagggctactacaaccaagccgagggctggaagtggggcggctgctcc
gccgacgtgcgttacggcatcgacttctcccggcgcttcgtggacgctcgggagatcaag
aagaacgcgcggcgcctcatgaacctgcataacaatgaggccggcaggaaggttctagag
gaccggatgcagctggagtgcaagtgccacggcgtgtctggctcctgcaccaccaaaacc
tgctggaccacgctgcccaagttccgagaggtgggccacctgctgaaggagaagtacaac
gcggccgtgcaggtggaggtggtgcgggccagccgtctgcggcagcccaccttcctgcgc
atcaaacagctgcgcagctatcagaagcccatggagacagacctggtgtacattgagaag
tcgcccaactactgcgaggaggacgcggccacgggcagcgtgggcacgcagggccgtctc
tgcaaccgcacgtcgcccggcgcggacggctgtgacaccatgtgctgcggccgaggctac
aacacccaccagtacaccaaggtgtggcagtgcaactgcaaattccactggtgctgcttc
gtcaagtgcaacacctgcagcgagcgcaccgaggtcttcacctgcaagtga
DBGET
integrated database retrieval system