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OXA1
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Skeletal muscle psoas
Extraocular muscle
Macrophage of peripheral blood
B lymphocyte (IgM memory) of spleen
B lymphocyte (naive) of spleen
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Disease Atlas
Most Correlated Diseases
Sepsis due to Serratia
Injury of eye region
Developmental delay
Caseating tuberculoid granuloma
Systemic infection
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Pharmaco Atlas
Most Correlated Compounds
3-deazaneplanocin A
NVP-TAE684
dasatinib
telocinobufagin
TGX 221
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Knockdown Atlas
Most Correlated Gene Perturbations
DOT1
rde-4
MIR122
ATP5F1B
IQGAP1
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
The ER membrane complex (EMC) can functionally replace the Oxa1 insertase in mitochondria.
Purification of Mitochondrial Ribosomes with the Translocase Oxa1L from HEK Cells.
OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.
Identification of Oxa1 Homologs Operating in the Eukaryotic Endoplasmic Reticulum.
Structural and molecular mechanisms for membrane protein biogenesis by the Oxa1 superfamily.
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Clinical Trials
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