NDE1 Chromosome 16

NudE neurodevelopment protein 1
22 variants 22 Health Risk

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What This Gene Does
This gene encodes a member of the nuclear distribution E (NudE) family of proteins. The encoded protein is localized at the centrosome and interacts with other centrosome components as part of a multiprotein complex that regulates dynein function. This protein plays an essential role in microtubule organization, mitosis and neuronal migration. Mutations in this gene cause lissencephaly 4, a disorder characterized by lissencephaly, severe brain atrophy, microcephaly, and severe cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]
Gene Info
Gene Group
MicroRNA protein coding host genes
Locus Type
gene with protein product
Location
16p13.11
Ensembl
ENSG00000072864
Associated Conditions (5)
Lissencephaly 4
NDE1-related microhydranencephaly
Intellectual disability
Inborn genetic diseases
NDE1-related disorder
Key Variants
All Variants (22)
RSID Category Clinical Significance Conditions
RS1123418 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Lissencephaly 4
RS146284370 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, NDE1-related microhydranencephaly, Intellectual disability
RS147174812 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Lissencephaly 4
RS147283674 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Inborn genetic diseases, Lissencephaly 4
RS149046258 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Lissencephaly 4
RS150492774 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Lissencephaly 4
RS201783071 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Lissencephaly 4
RS373842185 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS376548563 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, NDE1-related disorder, Lissencephaly 4
RS538373943 Health Risk Conflicting classifications of pathogenicity
RS570994490 Health Risk Conflicting classifications of pathogenicity NDE1-related disorder, NDE1-related disorder
RS572790932 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Lissencephaly 4
RS760012847 Health Risk Conflicting classifications of pathogenicity Lissencephaly 4, Lissencephaly 4
RS794727491 Health Risk Conflicting classifications of pathogenicity
RS794727785 Health Risk Conflicting classifications of pathogenicity
RS1456594953 Health Risk Pathogenic Lissencephaly 4, Lissencephaly 4
RS2151436194 Health Risk Pathogenic NDE1-related microhydranencephaly, Lissencephaly 4, NDE1-related microhydranencephaly
RS398123577 Health Risk Pathogenic
RS749768828 Health Risk Pathogenic Lissencephaly 4, NDE1-related disorder, Lissencephaly 4
RS756206942 Health Risk Pathogenic Lissencephaly 4, NDE1-related microhydranencephaly, Lissencephaly 4
RS757604577 Health Risk Pathogenic Lissencephaly 4, Lissencephaly 4
RS576928842 Health Risk Pathogenic/Likely pathogenic Lissencephaly 4, Lissencephaly 4
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