NEDD4L Chromosome 18
NEDD4 like E3 ubiquitin protein ligase
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What This Gene Does
This gene encodes a member of the Nedd4 family of HECT domain E3 ubiquitin ligases. HECT domain E3 ubiquitin ligases transfer ubiquitin from E2 ubiquitin-conjugating enzymes to protein substrates, thus targeting specific proteins for lysosomal degradation. The encoded protein mediates the ubiquitination of multiple target substrates and plays a critical role in epithelial sodium transport by regulating the cell surface expression of the epithelial sodium channel, ENaC. Single nucleotide polymorphisms in this gene may be associated with essential hypertension. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]
Gene Info
Gene Group
"C2 domain containing|Nedd4 family E3 ubiquitin protein ligases"
Locus Type
gene with protein product
Location
18q21.31
Ensembl
ENSG00000049759
Associated Conditions (9)
Inborn genetic diseases
Periventricular nodular heterotopia 7
Intellectual disability
NEDD4L-related disorder
Colon adenocarcinoma
Periventricular nodular heterotopia with syndactyly
cleft palate and developmental delay
Chromosome 5Q14.3 deletion syndrome
distal
Key Variants
RS1057524052
Conflicting classifications of pathogenicity
Health Risk
RS1178688498
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1383247620
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1404724194
Conflicting classifications of pathogenicity
Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
Health Risk
RS141078303
Conflicting classifications of pathogenicity
Inborn genetic diseases, Periventricular nodular heterotopia 7, Inborn genetic diseases
Health Risk
RS1455899867
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1477791039
Conflicting classifications of pathogenicity
Periventricular nodular heterotopia 7, Inborn genetic diseases, Periventricular nodular heterotopia 7
Health Risk
RS200565814
Conflicting classifications of pathogenicity
Periventricular nodular heterotopia 7, Intellectual disability, Periventricular nodular heterotopia 7
Health Risk
RS202127939
Conflicting classifications of pathogenicity
Periventricular nodular heterotopia 7, Inborn genetic diseases, Periventricular nodular heterotopia 7
Health Risk
RS2042365082
Conflicting classifications of pathogenicity
Health Risk
RS2059009080
Conflicting classifications of pathogenicity
Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
Health Risk
RS2059009305
Conflicting classifications of pathogenicity
NEDD4L-related disorder, Inborn genetic diseases, NEDD4L-related disorder
Health Risk
All Variants (52)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS2059194330 | Health Risk | Pathogenic/Likely pathogenic | Periventricular nodular heterotopia 7, Intellectual disability, Periventricular nodular heterotopia 7 |
| RS879255597 | Health Risk | Pathogenic/Likely pathogenic | Periventricular nodular heterotopia with syndactyly, cleft palate and developmental delay, Periventricular nodular heterotopia 7 |