SLC25A16
- Aliases
-
- D10S105E
- GDA
- GDC
- Graves disease autoantigen
- HGT.1
- ML7
- Mitochondrial solute carrier protein homolog
- SLC25A16
- Solute carrier family 25 member 16
- graves disease autoantigen
- graves disease carrier protein
- hML7
- mitochondrial solute carrier protein homolog
- solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16
- solute carrier family 25 member 16
- Description
- SLC25A16 is a member of the mitochondrial carrier family and contains three tandemly repeated mitochondrial carrier protein domains. The SLC26A16 protein is found in the inner membrane of the mitochondria where it is necessary for the accumulation of coenzyme A in the mitochondrial matrix. SLC25A16 also facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. The SLC25A16 gene is thought to be involved in Graves' disease.
Attributes
- QA State
- Curated
- Type
- Protein
- HGNC Name
- SLC25A16
- Certifications
-
- None
- QA State for Breast
- Under Review
Non-Public Biomarker
Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.
Non-Public Biomarker
Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.
- Development and validation of sandwich ELISA microarrays with minimal assay interference.
- Discovery and preliminary confirmation of novel early detection biomarkers for triple-negative breast cancer using preclinical plasma samples from the Women's Health Initiative observational study.
- Plasma biomarker profiles differ depending on breast cancer subtype but RANTES is consistently increased.
Non-Public Biomarker
Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.