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Gene Gene information from NCBI Gene database.
Entrez ID 51629
Gene name Solute carrier family 25 member 39
Gene symbol SLC25A39
Synonyms (NCBI Gene)
CGI-69CGI69
Chromosome 17
Chromosome location 17q21.31
Summary This gene encodes a member of the SLC25 transporter or mitochondrial carrier family of proteins. Members of this family are encoded by the nuclear genome while their protein products are usually embedded in the inner mitochondrial membrane and exhibit wid
miRNA miRNA information provided by mirtarbase database.
212 Show/Hide all (212)
miRTarBase ID miRNA Experiments Reference
MIRT022636 hsa-miR-124-3p Microarray 18668037
MIRT025628 hsa-miR-7-5p Microarray 19073608
MIRT025628 hsa-miR-7-5p Sequencing 20371350
MIRT027062 hsa-miR-103a-3p Sequencing 20371350
MIRT031718 hsa-miR-16-5p Sequencing 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18 Show/Hide all (18)
GO ID Ontology Definition Evidence Reference
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IBA
GO:0005739 Component Mitochondrion IEA
GO:0005743 Component Mitochondrial inner membrane IDA 11256614, 37917749
GO:0005743 Component Mitochondrial inner membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610820 24279 ENSG00000013306
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BZJ4
Protein name Mitochondrial glutathione transporter SLC25A39 (Solute carrier family 25 member 39)
Protein function Mitochondrial transporter required for glutathione import into mitochondria (PubMed:34707288, PubMed:35513392, PubMed:37917749, PubMed:38157846). Glutathione, which plays key roles in oxidative metabolism, is produced exclusively in the cytosol
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00153 Mito_carr 7 → 156 Mitochondrial carrier protein Family
PF00153 Mito_carr 251 → 352 Mitochondrial carrier protein Family
PF00153 Mito_carr 158 → 248 Mitochondrial carrier protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in many tissues (PubMed:11139402). Abundant in testis and kidney (PubMed:11139402). {ECO:0000269|PubMed:11139402}.
Sequence
Sequence length 359
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
EBV-positive nodal T- and NK-cell lymphoma Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Neoplasms Breast neoplasm Pubtator 33691015 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Glomerulonephritis Glomerulonephritis Pubtator 40186888 Inhibit
★★★★★
★☆☆☆☆
Found in Text Mining only
Kidney Diseases Kidney disease Pubtator 40186888 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Parkinson disease Pubtator 34148545 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Sarcoma Sarcoma Pubtator 33963205 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only