ATG7 Chromosome 3

Autophagy related 7
8 variants 8 Health Risk

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What This Gene Does
This gene encodes an E1-like activating enzyme that is essential for autophagy and cytoplasmic to vacuole transport. The encoded protein is also thought to modulate p53-dependent cell cycle pathways during prolonged metabolic stress. It has been associated with multiple functions, including axon membrane trafficking, axonal homeostasis, mitophagy, adipose differentiation, and hematopoietic stem cell maintenance. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015]
Gene Info
Gene Group
"Ubiquitin like modifier activating enzymes|Autophagy related"
Locus Type
gene with protein product
Location
3p25.3
Ensembl
ENSG00000197548
Associated Conditions (4)
NAFLD1
Spinocerebellar ataxia
autosomal recessive 31
Nonpapillary renal cell carcinoma
Key Variants
All Variants (8)
RSID Category Clinical Significance Conditions
RS143545741 Health Risk Conflicting classifications of pathogenicity NAFLD1, Spinocerebellar ataxia, autosomal recessive 31
RS146589465 Health Risk Conflicting classifications of pathogenicity
RS142493104 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive 31, Spinocerebellar ataxia
RS200074530 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive 31, Nonpapillary renal cell carcinoma
RS2152756968 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive 31, Spinocerebellar ataxia
RS2152811529 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive 31, Spinocerebellar ataxia
RS777067201 Health Risk Pathogenic Spinocerebellar ataxia, autosomal recessive 31, Spinocerebellar ataxia
RS201706487 Health Risk Pathogenic/Likely pathogenic Spinocerebellar ataxia, autosomal recessive 31, Spinocerebellar ataxia
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