Human Gene DVL1 (ENST00000378891.9) from GENCODE V44
  Description: Homo sapiens dishevelled segment polarity protein 1 (DVL1), transcript variant 2, mRNA. (from RefSeq NM_004421)
RefSeq Summary (NM_004421): 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].
Gencode Transcript: ENST00000378891.9
Gencode Gene: ENSG00000107404.21
Transcript (Including UTRs)
   Position: hg38 chr1:1,335,276-1,349,112 Size: 13,837 Total Exon Count: 15 Strand: -
Coding Region
   Position: hg38 chr1:1,336,142-1,349,065 Size: 12,924 Coding Exon Count: 15 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesGeneReviewsMethods
Data last updated at UCSC: 2023-08-18 00:09:47

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr1:1,335,276-1,349,112)mRNA (may differ from genome)Protein (670 aa)
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HGNCHPRDLynxMalacardsMGIneXtProt
OMIMPubMedReactomeUniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: DVL1_HUMAN
DESCRIPTION: RecName: Full=Segment polarity protein dishevelled homolog DVL-1; Short=Dishevelled-1; AltName: Full=DSH homolog 1;
FUNCTION: Participates in Wnt signaling by binding to the cytoplasmic C-terminus of frizzled family members and transducing the Wnt signal to down-stream effectors. Plays a role both in canonical and non-canonical Wnt signaling. Plays a role in the signal transduction pathways mediated by multiple Wnt genes. Required for LEF1 activation upon WNT1 and WNT3A signaling. DVL1 and PAK1 form a ternary complex with MUSK which is important for MUSK-dependent regulation of AChR clustering during the formation of the neuromuscular junction (NMJ).
SUBUNIT: Interacts with CXXC4. Interacts (via PDZ domain) with NXN (By similarity). Interacts with BRD7 and INVS. Interacts through its PDZ domain with the C-terminal regions of VANGL1, VANGL2 and CCDC88C/DAPLE. Interacts with ARRB1; the interaction is enhanced by phosphorylation of DVL1. Interacts with CYLD (By similarity). Interacts (via PDZ domain) with RYK. Self-associates (via DIX domain) and forms higher homooligomers. Interacts (via PDZ domain) with DACT1 and FZD7, where DACT1 and FZD7 compete for the same binding site (By similarity). Interacts (via DEP domain) with MUSK; the interaction is direct and mediates the formation a DVL1, MUSK and PAK1 ternary complex involved in AChR clustering (By similarity).
SUBCELLULAR LOCATION: Cell membrane; Peripheral membrane protein; Cytoplasmic side (By similarity). Cytoplasm, cytosol (By similarity). Cytoplasmic vesicle (By similarity). Note=Localizes at the cell membrane upon interaction with frizzled family members (By similarity).
DOMAIN: The DIX domain promotes homooligomerization (By similarity).
DOMAIN: The DEP domain mediates interaction with the cell membrane (By similarity).
PTM: Ubiquitinated; undergoes both 'Lys-48'-linked ubiquitination, leading to its subsequent degradation by the ubiquitin-proteasome pathway, and 'Lys-63'-linked ubiquitination. The interaction with INVS is required for ubiquitination. Deubiquitinated by CYLD, which acts on 'Lys-63'-linked ubiquitin chains (By similarity).
SIMILARITY: Belongs to the DSH family.
SIMILARITY: Contains 1 DEP domain.
SIMILARITY: Contains 1 DIX domain.
SIMILARITY: Contains 1 PDZ (DHR) domain.

-  Primer design for this transcript
 

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-  MalaCards Disease Associations
  MalaCards Gene Search: DVL1
Diseases sorted by gene-association score: robinow syndrome, autosomal dominant 2* (1024), autosomal dominant robinow syndrome* (261), charcot-marie-tooth disease type 2a (20), robinow syndrome (17), neural tube defects (3), nephronophthisis (2), colorectal cancer (2)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 67.84 RPKM in Muscle - Skeletal
Total median expression: 1522.70 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -21.6047-0.460 Picture PostScript Text
3' UTR -404.60866-0.467 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR000591 - DEP_dom
IPR008340 - Dishevelled_1
IPR024580 - Dishevelled_C-dom
IPR008339 - Dishevelled_fam
IPR003351 - Dishevelled_protein_dom
IPR001158 - DIX
IPR015506 - Dsh/Dvl-rel
IPR001478 - PDZ
IPR011991 - WHTH_trsnscrt_rep_DNA-bd

Pfam Domains:
PF00610 - Domain found in Dishevelled, Egl-10, and Pleckstrin (DEP)
PF02377 - Dishevelled specific domain
PF00778 - DIX domain
PF12316 - Segment polarity protein dishevelled (Dsh) C terminal
PF00595 - PDZ domain (Also known as DHR or GLGF)

ModBase Predicted Comparative 3D Structure on O14640
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-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
Genome BrowserGenome BrowserGenome BrowserNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
MGIRGDEnsembl   
Protein SequenceProtein SequenceProtein Sequence   
AlignmentAlignmentAlignment   

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005109 frizzled binding
GO:0005515 protein binding
GO:0008013 beta-catenin 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:0001934 positive 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:0007275 multicellular organism development
GO:0007409 axonogenesis
GO:0007411 axon guidance
GO:0007528 neuromuscular junction development
GO:0010976 positive regulation of neuron projection development
GO:0016055 Wnt signaling pathway
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:0035567 non-canonical Wnt signaling pathway
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:0050821 protein stabilization
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:0060997 dendritic spine morphogenesis
GO:0071340 skeletal muscle acetylcholine-gated channel clustering
GO:0090090 negative regulation of canonical Wnt signaling pathway
GO:0090103 cochlea morphogenesis
GO:0090179 planar cell polarity pathway involved in neural tube closure
GO:0090263 positive regulation of canonical Wnt signaling pathway
GO:0099054 presynapse assembly
GO:1903827 regulation of cellular protein localization
GO:1904886 beta-catenin destruction complex disassembly
GO:1905386 positive regulation of protein localization to presynapse
GO:2000463 positive regulation of excitatory postsynaptic potential

Cellular Component:
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0005874 microtubule
GO:0005886 plasma membrane
GO:0014069 postsynaptic density
GO:0015630 microtubule cytoskeleton
GO:0016020 membrane
GO:0030136 clathrin-coated vesicle
GO:0030424 axon
GO:0030425 dendrite
GO:0030426 growth cone
GO:0031410 cytoplasmic vesicle
GO:0043005 neuron projection
GO:0043025 neuronal cell body
GO:0043197 dendritic spine
GO:0045202 synapse
GO:0098793 presynapse
GO:1990909 Wnt signalosome
GO:0016328 lateral plasma membrane


-  Descriptions from all associated GenBank mRNAs
  BC017225 - Homo sapiens dishevelled, dsh homolog 1 (Drosophila), mRNA (cDNA clone IMAGE:4299758), partial cds.
AF006011 - Homo sapiens dishevelled 1 (DVL1) mRNA, complete cds.
BC025292 - Homo sapiens cDNA clone IMAGE:4554266, containing frame-shift errors.
BC050454 - Homo sapiens dishevelled, dsh homolog 1 (Drosophila), mRNA (cDNA clone MGC:54245 IMAGE:6201003), complete cds.
AK093189 - Homo sapiens cDNA FLJ35870 fis, clone TESTI2007998, highly similar to SEGMENT POLARITY PROTEIN DISHEVELLED HOMOLOG DVL-1.
AX747980 - Sequence 1505 from Patent EP1308459.
AK095867 - Homo sapiens cDNA FLJ38548 fis, clone HCHON2001768, highly similar to Segment polarity protein dishevelled homolog DVL-1.
AB209210 - Homo sapiens mRNA for dishevelled 1 isoform a variant protein.
JD481672 - Sequence 462696 from Patent EP1572962.
BC111419 - Homo sapiens cDNA clone IMAGE:40023756.
JD495614 - Sequence 476638 from Patent EP1572962.
AK300063 - Homo sapiens cDNA FLJ56879 complete cds, highly similar to Segment polarity protein dishevelled homolog DVL-1.
AK293286 - Homo sapiens cDNA FLJ56847 complete cds, highly similar to Segment polarity protein dishevelled homologDVL-1.
JD401344 - Sequence 382368 from Patent EP1572962.
U46461 - Human dishevelled homolog (DVL) mRNA, complete cds.
KJ901396 - Synthetic construct Homo sapiens clone ccsbBroadEn_10790 DVL1 gene, encodes complete protein.
AB385564 - Synthetic construct DNA, clone: pF1KB8019, Homo sapiens DVL1 gene for segment polarity protein dishevelled homolog DVL-1, complete cds, without stop codon, in Flexi system.
CU690690 - Synthetic construct Homo sapiens gateway clone IMAGE:100021370 5' read DVL1 mRNA.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa04310 - Wnt signaling pathway
hsa04330 - Notch signaling pathway
hsa04916 - Melanogenesis
hsa05200 - Pathways in cancer
hsa05217 - Basal cell carcinoma

BioCarta from NCI Cancer Genome Anatomy Project
h_alkPathway - ALK in cardiac myocytes
h_hesPathway - Segmentation Clock
h_pitx2Pathway - Multi-step Regulation of Transcription by Pitx2
h_agrPathway - Agrin in Postsynaptic Differentiation
h_ps1Pathway - Presenilin action in Notch and Wnt signaling
h_gsk3Pathway - Inactivation of Gsk3 by AKT causes accumulation of b-catenin in Alveolar Macrophages
h_wntPathway - WNT Signaling Pathway

Reactome (by CSHL, EBI, and GO)

Protein O14640 (Reactome details) participates in the following event(s):

R-HSA-4641155 DVL1 is bound by the HECT ubiquitin ligase HECW1
R-HSA-4641159 DVL1 is ubiquitinated by HECW1
R-HSA-201717 CSNK2-mediated phosphorylation of DVL
R-HSA-1504213 DVL is bound by the CUL3:KLHL12:RBX1 ubiquitin ligase complex
R-HSA-5368582 CXXC4 binds DVL to prevent AXIN binding
R-NUL-5368583 Cxxc4 binds DVL to prevent AXIN binding
R-NUL-5368587 DVL binds Ccdc88c
R-HSA-5368588 DVL binds CCDC88C
R-HSA-3772435 WNT signaling stimulates CSNK1-dependent phosphorylation of DVL
R-HSA-3858482 DVL is recruited to the receptor
R-HSA-1504188 FZD recruits DVL to the receptor complex
R-HSA-3772434 Phosphorylated DVL recruits PIP5K1B to the plasma membrane
R-HSA-3858475 ppDVL recruits RAC
R-HSA-3858489 ppDVL binds DAAM1
R-HSA-3858480 WNT-dependent phosphorylation of DVL
R-HSA-1504190 DVL is ubiquitinated by CUL3:KLHL12:RBX1
R-HSA-201691 Phosphorylation of LRP5/6 cytoplasmic domain by CSNKI
R-NUL-1458902 frog CK1gamma phosphorylates LRP5/6
R-HSA-201677 Phosphorylation of LRP5/6 cytoplasmic domain by membrane-associated GSK3beta
R-HSA-1504186 DVL recruits GSK3beta:AXIN1 to the receptor complex
R-HSA-3858495 DAAM1 recruits GTP-bound RHOA
R-HSA-3965450 DAAM1 recruits PFN1
R-HSA-3772436 DVL-associated PIP5K1B phosphorylates PI4P to PI(4,5)P2
R-HSA-4641258 Degradation of DVL
R-HSA-201688 WNT mediated activation of DVL
R-HSA-5368598 Negative regulation of TCF-dependent signaling by DVL-interacting proteins
R-HSA-201681 TCF dependent signaling in response to WNT
R-HSA-4086400 PCP/CE pathway
R-HSA-5663220 RHO GTPases Activate Formins
R-HSA-195721 Signaling by WNT
R-HSA-3858494 Beta-catenin independent WNT signaling
R-HSA-4641262 Disassembly of the destruction complex and recruitment of AXIN to the membrane
R-HSA-195258 RHO GTPase Effectors
R-HSA-162582 Signal Transduction
R-HSA-194315 Signaling by Rho GTPases

-  Other Names for This Gene
  Alternate Gene Symbols: DVL1_HUMAN, ENST00000378891.1, ENST00000378891.2, ENST00000378891.3, ENST00000378891.4, ENST00000378891.5, ENST00000378891.6, ENST00000378891.7, ENST00000378891.8, NM_004421, O14640, Q5TA33, Q5TA35, uc001aer.1, uc001aer.2, uc001aer.3, uc001aer.4, uc001aer.5
UCSC ID: ENST00000378891.9
RefSeq Accession: NM_004421
Protein: O14640 (aka DVL1_HUMAN)
CCDS: CCDS22.1, CCDS81252.1

-  GeneReviews for This Gene
  GeneReviews article(s) related to gene DVL1:
rob-ad (Autosomal Dominant Robinow Syndrome)

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.