ATAD3A Chromosome 1

ATPase family AAA domain containing 3A
41 variants 41 Health Risk

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What This Gene Does
This gene encodes a ubiquitously expressed mitochondrial membrane protein that contributes to mitochondrial dynamics, nucleoid organization, protein translation, cell growth, and cholesterol metabolism. This gene is a member of the ATPase family AAA-domain containing 3 gene family which, in humans, includes two other paralogs. Naturally occurring mutations in this gene are associated with distinct neurological syndromes including Harel-Yoon syndrome. High-level expression of this gene is associated with poor survival in breast cancer patients. A homozygous knockout of the orthologous gene in mice results in embryonic lethality at day 7.5 due to growth retardation and defective development of the trophoblast lineage. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]
Gene Info
Gene Group
"AAA ATPases|Mitochondrial nucleoid associated proteins"
Locus Type
gene with protein product
Location
1p36.33
Ensembl
ENSG00000197785
Associated Conditions (14)
Harel-Yoon syndrome
Pontocerebellar hypoplasia
hypotonia
and respiratory insufficiency syndrome
neonatal lethal
Inborn genetic diseases
Gastric cancer
Intellectual disability
Epilepsy
ATAD3A-related condition
Sarcoma
Disorder of development or morphogenesis
Acute myeloid leukemia
Congenital cerebellar hypoplasia
Key Variants
RS1057517687
Conflicting classifications of pathogenicity
Harel-Yoon syndrome, Pontocerebellar hypoplasia, hypotonia
Health Risk
RS1295527713
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1308954605
Conflicting classifications of pathogenicity
Inborn genetic diseases, Gastric cancer, Inborn genetic diseases
Health Risk
RS138007437
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS138594222
Conflicting classifications of pathogenicity
Harel-Yoon syndrome, Pontocerebellar hypoplasia, hypotonia
Health Risk
RS139254288
Conflicting classifications of pathogenicity
Inborn genetic diseases, Harel-Yoon syndrome, Inborn genetic diseases
Health Risk
RS148455993
Conflicting classifications of pathogenicity
Intellectual disability, Intellectual disability
Health Risk
RS200101143
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS200344678
Conflicting classifications of pathogenicity
Harel-Yoon syndrome, Inborn genetic diseases, Epilepsy
Health Risk
RS2100677960
Conflicting classifications of pathogenicity
Harel-Yoon syndrome, Inborn genetic diseases, Harel-Yoon syndrome
Health Risk
RS2478794
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS2524204010
Conflicting classifications of pathogenicity
ATAD3A-related condition, ATAD3A-related condition
Health Risk
All Variants (41)
RSID Category Clinical Significance Conditions
RS1057517687 Health Risk Conflicting classifications of pathogenicity Harel-Yoon syndrome, Pontocerebellar hypoplasia, hypotonia
RS1295527713 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1308954605 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Gastric cancer, Inborn genetic diseases
RS138007437 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS138594222 Health Risk Conflicting classifications of pathogenicity Harel-Yoon syndrome, Pontocerebellar hypoplasia, hypotonia
RS139254288 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Harel-Yoon syndrome, Inborn genetic diseases
RS148455993 Health Risk Conflicting classifications of pathogenicity Intellectual disability, Intellectual disability
RS200101143 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200344678 Health Risk Conflicting classifications of pathogenicity Harel-Yoon syndrome, Inborn genetic diseases, Epilepsy
RS2100677960 Health Risk Conflicting classifications of pathogenicity Harel-Yoon syndrome, Inborn genetic diseases, Harel-Yoon syndrome
RS2478794 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2524204010 Health Risk Conflicting classifications of pathogenicity ATAD3A-related condition, ATAD3A-related condition
RS2767471 Health Risk Conflicting classifications of pathogenicity Harel-Yoon syndrome, Pontocerebellar hypoplasia, hypotonia
RS2986576 Health Risk Conflicting classifications of pathogenicity
RS371490361 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Sarcoma, Harel-Yoon syndrome
RS41285840 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Disorder of development or morphogenesis, Intellectual disability
RS760598490 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Intellectual disability, Inborn genetic diseases
RS763685989 Health Risk Conflicting classifications of pathogenicity
RS766623034 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Harel-Yoon syndrome, Pontocerebellar hypoplasia
RS767198410 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Acute myeloid leukemia, Inborn genetic diseases
RS775070969 Health Risk Conflicting classifications of pathogenicity
RS780466539 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Harel-Yoon syndrome, Pontocerebellar hypoplasia
RS1172676832 Health Risk Likely pathogenic Harel-Yoon syndrome, Harel-Yoon syndrome
RS1212229540 Health Risk Likely pathogenic
RS1394640737 Health Risk Likely pathogenic
RS1464547304 Health Risk Likely pathogenic Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome
RS1467255409 Health Risk Likely pathogenic
RS1641698007 Health Risk Likely pathogenic Harel-Yoon syndrome, Harel-Yoon syndrome
RS1641722871 Health Risk Likely pathogenic Harel-Yoon syndrome, Harel-Yoon syndrome
RS2524128308 Health Risk Likely pathogenic Harel-Yoon syndrome, Pontocerebellar hypoplasia, hypotonia
RS2524212771 Health Risk Likely pathogenic Harel-Yoon syndrome, Harel-Yoon syndrome
RS755120064 Health Risk Likely pathogenic
RS757205195 Health Risk Likely pathogenic
RS762349361 Health Risk Likely pathogenic
RS902213391 Health Risk Likely pathogenic Harel-Yoon syndrome, Harel-Yoon syndrome
RS1557458134 Health Risk Pathogenic Harel-Yoon syndrome, Pontocerebellar hypoplasia, hypotonia
RS1570319915 Health Risk Pathogenic Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome
RS1570345942 Health Risk Pathogenic Congenital cerebellar hypoplasia, Pontocerebellar hypoplasia, hypotonia
RS374071750 Health Risk Pathogenic
RS760826883 Health Risk Pathogenic Pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome
RS1057517686 Health Risk Pathogenic/Likely pathogenic Harel-Yoon syndrome, Harel-Yoon syndrome
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