Gene: SLC25A26

Alternate names for this Gene: COXPD28|SAMC

Gene Summary: This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms.

Gene is located in Chromosome: 3

Location in Chromosome : 3p14.1

Description of this Gene: solute carrier family 25 member 26

Type of Gene: protein-coding

rs6781752 in SLC25A26 gene and Adenocarcinoma of large intestine PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs6781752 in SLC25A26 gene and Adenoma of large intestine PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs332388 in SLC25A26 gene and Atrial Fibrillation PMID 29892015 2018 Multi-ethnic genome-wide association study for atrial fibrillation.

rs145763646 in SLC25A26 gene and Bipolar Disorder PMID 29391396 2018 Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8.

rs7626079 in SLC25A26 gene and Body mass index PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs145763646 in SLC25A26 gene and Bulimia PMID 29391396 2018 Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8.

rs6781752 in SLC25A26 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs6781752 in SLC25A26 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs6781752 in SLC25A26 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs6781752 in SLC25A26 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs869025313 in SLC25A26 gene and COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28 PMID 26522469 2015 Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26.

rs6781752 in SLC25A26 gene and Colorectal Carcinoma PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs6781752 in SLC25A26 gene and Colorectal Neoplasms PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs6781752 in SLC25A26 gene and Malignant neoplasm of large intestine PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs6781752 in SLC25A26 gene and Malignant tumor of colon PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs332388 in SLC25A26 gene and RDW - Red blood cell distribution width result PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs332388 in SLC25A26 gene and Red cell distribution width determination PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.