ATAD3A Chromosome 1
ATPase family AAA domain containing 3A
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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 |