Homo sapiens (human): 1855
Help
Entry
1855 CDS
T01001
Symbol
DVL1, DRS2, DVL, DVL1L1, DVL1P1
Name
(RefSeq) dishevelled segment polarity protein 1
KO
K02353
segment polarity protein dishevelled
Organism
hsa
Homo sapiens (human)
Pathway
hsa04150
mTOR signaling pathway
hsa04310
Wnt signaling pathway
hsa04330
Notch signaling pathway
hsa04390
Hippo signaling pathway
hsa04550
Signaling pathways regulating pluripotency of stem cells
hsa04916
Melanogenesis
hsa04934
Cushing syndrome
hsa05010
Alzheimer disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05165
Human papillomavirus infection
hsa05200
Pathways in cancer
hsa05217
Basal cell carcinoma
hsa05224
Breast cancer
hsa05225
Hepatocellular carcinoma
hsa05226
Gastric cancer
Network
nt06164
Kaposi sarcoma-associated herpesvirus (KSHV)
nt06181
Salmonella
nt06215
WNT signaling (cancer)
nt06260
Colorectal cancer
nt06261
Gastric cancer
nt06263
Hepatocellular carcinoma
nt06270
Breast cancer
nt06271
Endometrial cancer
nt06274
Thyroid cancer
nt06505
WNT signaling
Element
N00056
Wnt signaling pathway
N00059
FZD7-overexpression to Wnt signaling pathway
N00060
LRP6-overexpression to Wnt signaling pathway
N01427
WNT5A-ROR signaling pathway
N01444
NXN mutation to WNT5A-ROR signaling pathway
Disease
H00485
Robinow syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
1855 (DVL1)
04330 Notch signaling pathway
1855 (DVL1)
04390 Hippo signaling pathway
1855 (DVL1)
04150 mTOR signaling pathway
1855 (DVL1)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
1855 (DVL1)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
1855 (DVL1)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
1855 (DVL1)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
1855 (DVL1)
05226 Gastric cancer
1855 (DVL1)
05217 Basal cell carcinoma
1855 (DVL1)
05224 Breast cancer
1855 (DVL1)
09172 Infectious disease: viral
05165 Human papillomavirus infection
1855 (DVL1)
09164 Neurodegenerative disease
05010 Alzheimer disease
1855 (DVL1)
05022 Pathways of neurodegeneration - multiple diseases
1855 (DVL1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
1855 (DVL1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Dsh_C
Dishevelled
DIX
PDZ
DEP
PDZ_6
Shufflon_N
Motif
Other DBs
NCBI-GeneID:
1855
NCBI-ProteinID:
NP_001317240
OMIM:
601365
HGNC:
3084
Ensembl:
ENSG00000107404
UniProt:
O14640
Structure
PDB
LinkDB
All DBs
Position
1:complement(1335278..1349418)
Genome browser
AA seq
695 aa
AA seq
DB search
MAETKIIYHMDEEETPYLVKLPVAPERVTLADFKNVLSNRPVHAYKFFFKSMDQDFGVVK
EEIFDDNAKLPCFNGRVVSWLVLAEGAHSDAGSQGTDSHTDLPPPLERTGGIGDSRPPSF
HPNVASSRDGMDNETGTESMVSHRRERARRRNREEAARTNGHPRGDRRRDVGLPPDSAST
ALSSELESSSFVDSDEDGSTSRLSSSTEQSTSSRLIRKHKRRRRKQRLRQADRASSFSSI
TDSTMSLNIVTVTLNMERHHFLGISIVGQSNDRGDGGIYIGSIMKGGAVAADGRIEPGDM
LLQVNDVNFENMSNDDAVRVLREIVSQTGPISLTVAKCWDPTPRSYFTVPRADPVRPIDP
AAWLSHTAALTGALPRYGTSPCSSAVTRTSSSSLTSSVPGAPQLEEAPLTVKSDMSAVVR
VMQLPDSGLEIRDRMWLKITIANAVIGADVVDWLYTHVEGFKERREARKYASSLLKHGFL
RHTVNKITFSEQCYYVFGDLCSNLATLNLNSGSSGTSDQDTLAPLPHPAAPWPLGQGYPY
QYPGPPPCFPPAYQDPGFSYGSGSTGSQQSEGSKSSGSTRSSRRAPGREKERRAAGAGGS
GSESDHTAPSGVGSSWRERPAGQLSRGSSPRSQASATAPGLPPPHPTTKAYTVVGGPPGG
PPVRELAAVPPELTGSRQSFQKAMGNPCEFFVDIM
NT seq
2088 nt
NT seq
+upstream
nt +downstream
nt
atggcggagaccaagattatctaccacatggacgaggaggagacgccgtacctggtcaag
ctgcccgtggcccccgagcgcgtcacgctggccgacttcaagaacgtgctcagcaaccgg
cccgtgcacgcctacaaattcttctttaagtccatggaccaggacttcggggtggtgaag
gaggagatctttgatgacaatgccaagcttccctgcttcaacggccgcgtggtctcctgg
ctggtcctggctgagggtgctcactcggatgcggggtcccagggcacggacagccacaca
gacctgcccccgcctcttgagcggacaggcggcatcggggactcccggcccccctccttc
cacccaaatgtggccagcagccgtgacgggatggacaacgagacaggcacggagtccatg
gtcagtcaccggcgggagcgtgcccgacgccggaaccgcgaggaggccgcccggaccaat
gggcacccaaggggagaccgacggcgggatgtggggctgcccccagacagcgcgtccacc
gccctcagcagcgagcttgagtccagcagctttgtggactcggacgaggatggcagcacg
agcaggctcagcagctccacggagcagagcacctcatccagactcatccggaagcacaaa
cgccggcggaggaagcagcgccttcggcaggcggaccgggcctcctccttcagcagcata
accgactccaccatgtccctcaacatcgtcactgtcacgctcaacatggaaagacatcac
tttctgggcatcagcatcgtggggcagagcaacgaccgtggagacggcggcatctacatt
ggctccatcatgaagggcggggctgtggccgctgacggccgcatcgagcccggcgacatg
ttgctgcaggtgaatgacgtgaactttgagaacatgagcaatgacgatgccgtgcgggtg
ctgcgggagatcgtttcccagacggggcccatcagcctcactgtggccaagtgctgggac
ccaacgccccgaagctacttcaccgtcccacgggctgacccggtgcggcccatcgacccc
gccgcctggctgtcccacacggcggcactgacaggagccctgccccgctacggtacgagt
ccctgctccagcgccgtcacgcgcaccagctcctcctcactaaccagctccgtgcctggt
gctccacagctggaagaggcgccgctgacggtgaagagtgacatgagcgccgtcgtccgg
gtcatgcagctgccagactcgggactggagatccgcgaccgcatgtggctcaagatcacc
atcgccaatgccgtcatcggggcggacgtggtggactggctgtacacacacgtggagggc
ttcaaggagcggcgggaggcccggaagtacgccagcagcttgctgaagcacggcttcctg
cggcacacggtcaacaagatcaccttctccgagcagtgctactacgtcttcggggatctc
tgcagcaatctcgccaccctgaacctcaacagtggctccagtgggacttcggatcaggac
acgctggccccgctgccccacccggctgccccctggcctctgggtcagggctacccctac
cagtacccgggacccccaccctgcttcccgcctgcctaccaggacccgggctttagctat
ggcagcggcagcaccgggagtcagcagagtgaagggagcaaaagcagtgggtccacccgg
agcagccgccgggccccgggccgtgagaaggagcgtcgggcggcgggagctgggggcagt
ggcagtgaatcggatcacacggcaccgagtggggtggggagcagctggcgagagcgtccg
gccggccagctcagccgtggcagcagcccacgcagtcaggcctcggctaccgccccgggg
ctccccccgccccaccccacgaccaaggcctatacagtggtgggggggccacccggggga
ccccctgtccgggagctggctgccgtccccccggaattgacaggcagccgccagtccttc
cagaaggctatggggaacccctgcgagttcttcgtggacatcatgtga
DBGET
integrated database retrieval system