Gene Gene information from NCBI Gene database.
Entrez ID 399512
Gene name Solute carrier family 25 member 35
Gene symbol SLC25A35
Synonyms (NCBI Gene)
-
Chromosome 17
Chromosome location 17p13.1
Summary SLC25A35 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
40
miRTarBase ID miRNA Experiments Reference
MIRT1356446 hsa-miR-1280 CLIP-seq
MIRT1356447 hsa-miR-1915 CLIP-seq
MIRT1356448 hsa-miR-4258 CLIP-seq
MIRT1356449 hsa-miR-4270 CLIP-seq
MIRT1356450 hsa-miR-4441 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IEA
GO:0005743 Component Mitochondrial inner membrane IEA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610818 31921 ENSG00000125434
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q3KQZ1
Protein name Solute carrier family 25 member 35
Protein function Putative antiporter that exchanges dicarboxylates and sulfur oxoanions across the inner membrane of mitochondria.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00153 Mito_carr 1 90 Mitochondrial carrier protein Family
PF00153 Mito_carr 98 197 Mitochondrial carrier protein Family
PF00153 Mito_carr 202 299 Mitochondrial carrier protein Family
Sequence
Sequence length 300
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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 Evidence Score
CARDIAC ARRHYTHMIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLOMERULONEPHRITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
UTERINE FIBROID GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations