DVL3 Chromosome 3
Dishevelled segment polarity protein 3
Upload your DNA to see your personal genotypes for variants in DVL3.
What This Gene Does
This gene is a member of a multi-gene family which shares strong similarity with the Drosophila dishevelled gene, dsh. The Drosophila dishevelled gene encodes a cytoplasmic phosphoprotein that regulates cell proliferation. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Dishevelled segment polarity proteins|PDZ domain containing|DEP domain containing"
Locus Type
gene with protein product
Location
3q27.1
Ensembl
ENSG00000161202
Associated Conditions (7)
Inborn genetic diseases
DVL3-related disorder
Autosomal dominant Robinow syndrome 3
Autosomal dominant Robinow syndrome 2
See cases
11 conditions
Autosomal dominant Robinow syndrome 1
Key Variants
RS1049906925
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1167113982
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1172794619
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1402968787
Conflicting classifications of pathogenicity
Inborn genetic diseases, DVL3-related disorder, Inborn genetic diseases
Health Risk
RS146365513
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS146812695
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS151229784
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1687252
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS199853617
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS200798545
Conflicting classifications of pathogenicity
Inborn genetic diseases, Autosomal dominant Robinow syndrome 3, Inborn genetic diseases
Health Risk
RS201329929
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS201932377
Conflicting classifications of pathogenicity
Inborn genetic diseases, Autosomal dominant Robinow syndrome 3, Inborn genetic diseases
Health Risk
All Variants (34)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1049906925 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1167113982 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1172794619 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1402968787 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, DVL3-related disorder, Inborn genetic diseases |
| RS146365513 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS146812695 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS151229784 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1687252 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS199853617 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS200798545 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Autosomal dominant Robinow syndrome 3, Inborn genetic diseases |
| RS201329929 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS201932377 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Autosomal dominant Robinow syndrome 3, Inborn genetic diseases |
| RS371541138 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS371684582 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS528271179 | Health Risk | Conflicting classifications of pathogenicity | DVL3-related disorder, Inborn genetic diseases, DVL3-related disorder |
| RS765852473 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS767932262 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS768998141 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS769468812 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1553811652 | Health Risk | Likely pathogenic | Autosomal dominant Robinow syndrome 2, Autosomal dominant Robinow syndrome 2 |
| RS1714775017 | Health Risk | Likely pathogenic | — |
| RS2109022762 | Health Risk | Likely pathogenic | Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 3 |
| RS2109023862 | Health Risk | Likely pathogenic | Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 3 |
| RS2109023897 | Health Risk | Likely pathogenic | See cases, See cases |
| RS2473697428 | Health Risk | Likely pathogenic | Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 3 |
| RS753876000 | Health Risk | Likely pathogenic | 11 conditions, 11 conditions |
| RS869025217 | Health Risk | Likely pathogenic | Autosomal dominant Robinow syndrome 1, Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 2 |
| RS1577052471 | Health Risk | Pathogenic | Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 3 |
| RS1577052755 | Health Risk | Pathogenic | — |
| RS1577052785 | Health Risk | Pathogenic | Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 3 |
| RS869025215 | Health Risk | Pathogenic | Autosomal dominant Robinow syndrome 1, Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 2 |
| RS869025216 | Health Risk | Pathogenic | Autosomal dominant Robinow syndrome 1, Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 2 |
| RS869025218 | Health Risk | Pathogenic | Autosomal dominant Robinow syndrome 1, Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 2 |
| RS869025219 | Health Risk | Pathogenic | Autosomal dominant Robinow syndrome 1, Autosomal dominant Robinow syndrome 3, Autosomal dominant Robinow syndrome 2 |