NEDD4L Chromosome 18

NEDD4 like E3 ubiquitin protein ligase
52 variants 52 Health Risk

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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
RS1057524052 Health Risk Conflicting classifications of pathogenicity
RS1178688498 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1383247620 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1404724194 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS141078303 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Periventricular nodular heterotopia 7, Inborn genetic diseases
RS1455899867 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1477791039 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Inborn genetic diseases, Periventricular nodular heterotopia 7
RS200565814 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Intellectual disability, Periventricular nodular heterotopia 7
RS202127939 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Inborn genetic diseases, Periventricular nodular heterotopia 7
RS2042365082 Health Risk Conflicting classifications of pathogenicity
RS2059009080 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS2059009305 Health Risk Conflicting classifications of pathogenicity NEDD4L-related disorder, Inborn genetic diseases, NEDD4L-related disorder
RS2059726758 Health Risk Conflicting classifications of pathogenicity
RS2516870215 Health Risk Conflicting classifications of pathogenicity
RS367735608 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS371954364 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS372739641 Health Risk Conflicting classifications of pathogenicity
RS375068828 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375316659 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, NEDD4L-related disorder, Inborn genetic diseases
RS375898604 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Inborn genetic diseases, Periventricular nodular heterotopia 7
RS377143286 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Inborn genetic diseases, Periventricular nodular heterotopia 7
RS572854572 Health Risk Conflicting classifications of pathogenicity
RS747072217 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS747092381 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS748006260 Health Risk Conflicting classifications of pathogenicity Intellectual disability, Intellectual disability
RS748774036 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS748936457 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Colon adenocarcinoma, Periventricular nodular heterotopia 7
RS749019037 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS751509135 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS752858201 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS755525575 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS757461439 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS760992833 Health Risk Conflicting classifications of pathogenicity
RS763159512 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS764101138 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS766146854 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS767730323 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS769198983 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS771098028 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS773477776 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS775630982 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS781089843 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS879255596 Health Risk Conflicting classifications of pathogenicity Periventricular nodular heterotopia with syndactyly, cleft palate and developmental delay, Periventricular nodular heterotopia 7
RS907217983 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2046707868 Health Risk Likely pathogenic Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS2059723813 Health Risk Likely pathogenic Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS2146788855 Health Risk Likely pathogenic
RS2516772394 Health Risk Likely pathogenic Periventricular nodular heterotopia 7, Periventricular nodular heterotopia 7
RS879255598 Health Risk Pathogenic Periventricular nodular heterotopia with syndactyly, cleft palate and developmental delay, Periventricular nodular heterotopia 7
RS879255599 Health Risk Pathogenic Periventricular nodular heterotopia with syndactyly, cleft palate and developmental delay, Periventricular nodular heterotopia 7
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