Homo sapiens Gene: DVL1
InnateDB Gene IDBG-85121.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DVL1
Gene Name dishevelled, dsh homolog 1 (Drosophila)
Synonyms DVL; DVL1L1; DVL1P1;
Species Homo sapiens
Ensembl Gene ENSG00000107404
Encoded Proteins
dishevelled, dsh homolog 1 (Drosophila)
dishevelled, dsh homolog 1 (Drosophila)
dishevelled segment polarity protein 1
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary DVL1, the human homolog of the Drosophila dishevelled gene (dsh) encodes a cytoplasmic phosphoprotein that regulates cell proliferation, acting as a transducer molecule for developmental processes, including segmentation and neuroblast specification. DVL1 is a candidate gene for neuroblastomatous transformation. The Schwartz-Jampel syndrome and Charcot-Marie-Tooth disease type 2A have been mapped to the same region as DVL1. The phenotypes of these diseases may be consistent with defects which might be expected from aberrant expression of a DVL gene during development. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:1335276-1349350
Strand Reverse strand
Band p36.33
ENST00000378891 ENSP00000368169
ENST00000378888 ENSP00000368166
ENST00000610709 ENSP00000480077
Number of Interactions This gene and/or its encoded proteins are associated with 57 experimentally validated interaction(s) in this database.
They are also associated with 35 interaction(s) predicted by orthology.
Experimentally validated
Total 57 [view]
Protein-Protein 57 [view]
Protein-DNA 0
Protein-RNA 0
Predicted by orthology
Total 35 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004871 signal transducer activity
GO:0005109 frizzled binding
GO:0005515 protein binding
GO:0019899 enzyme binding
GO:0019901 protein kinase binding
GO:0042802 identical protein binding
GO:0048365 Rac GTPase binding
Biological Process
GO:0001505 regulation of neurotransmitter levels
GO:0001932 regulation of protein phosphorylation
GO:0001933 negative regulation of protein phosphorylation
GO:0006366 transcription from RNA polymerase II promoter
GO:0006469 negative regulation of protein kinase activity
GO:0007269 neurotransmitter secretion
GO:0007409 axonogenesis
GO:0007411 axon guidance
GO:0007528 neuromuscular junction development
GO:0010976 positive regulation of neuron projection development
GO:0021915 neural tube development
GO:0022007 convergent extension involved in neural plate elongation
GO:0030177 positive regulation of Wnt signaling pathway
GO:0031122 cytoplasmic microtubule organization
GO:0032091 negative regulation of protein binding
GO:0032436 positive regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:0034504 protein localization to nucleus
GO:0035176 social behavior
GO:0035372 protein localization to microtubule
GO:0035556 intracellular signal transduction
GO:0043113 receptor clustering
GO:0045893 positive regulation of transcription, DNA-templated
GO:0048668 collateral sprouting
GO:0048675 axon extension
GO:0048813 dendrite morphogenesis
GO:0050808 synapse organization
GO:0060026 convergent extension
GO:0060029 convergent extension involved in organogenesis
GO:0060070 canonical Wnt signaling pathway
GO:0060071 Wnt signaling pathway, planar cell polarity pathway
GO:0060134 prepulse inhibition
GO:0071340 skeletal muscle acetylcholine-gated channel clustering
GO:0090103 cochlea morphogenesis
GO:0090179 planar cell polarity pathway involved in neural tube closure
GO:0090263 positive regulation of canonical Wnt signaling pathway
Cellular Component
GO:0005829 cytosol
GO:0005874 microtubule
GO:0005938 cell cortex
GO:0015630 microtubule cytoskeleton
GO:0016023 cytoplasmic membrane-bounded vesicle
GO:0016328 lateral plasma membrane
GO:0030136 clathrin-coated vesicle
GO:0030424 axon
GO:0030425 dendrite
GO:0030426 growth cone
GO:0031410 cytoplasmic vesicle
GO:0043025 neuronal cell body
GO:0045202 synapse
Mus musculus
Bos taurus
Gene ID
Gene Order
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
TGF_beta_Receptor pathway
Wnt pathway
PCP/CE pathway pathway
WNT mediated activation of DVL pathway
negative regulation of TCF-dependent signaling by DVL-interacting proteins pathway
misspliced LRP5 mutants have enhanced beta-catenin-dependent signaling pathway
Signaling by WNT in cancer pathway
beta-catenin independent WNT signaling pathway
Signaling by Wnt pathway
disassembly of the destruction complex and recruitment of AXIN to the membrane pathway
degradation of DVL pathway
Signal Transduction pathway
TCF dependent signaling in response to WNT pathway
RNF mutants show enhanced WNT signaling and proliferation pathway
XAV939 inhibits tankyrase, stabilizing AXIN pathway
Disease pathway
Wnt signaling pathway pathway
Notch signaling pathway pathway
Melanogenesis pathway
Pathways in cancer pathway
Basal cell carcinoma pathway
Wnt signaling pathway pathway
Segmentation clock [Biocarta view]
Inactivation of gsk3 by akt causes accumulation of b-catenin in alveolar macrophages [Biocarta view]
Agrin in postsynaptic differentiation [Biocarta view]
Multi-step regulation of transcription by pitx2 [Biocarta view]
Wnt signaling pathway [Biocarta view]
Presenilin action in Notch and Wnt signaling
UniProt Splice Variant
Entrez Gene
UniGene Hs.731450 Hs.743700
RefSeq NM_004421 XM_005244731 XM_005244732 XM_005244733
HPRD 03220
RNA Seq Atlas