Gene Gene information from NCBI Gene database.
Entrez ID 10478
Gene name Solute carrier family 25 member 17
Gene symbol SLC25A17
Synonyms (NCBI Gene)
PMP34
Chromosome 22
Chromosome location 22q13.2
Summary This gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers. It is expressed in the liver, and is likely involved in transport. Alternative splicing results in multiple transcript variants. [provided by Ref
miRNA miRNA information provided by mirtarbase database.
273
miRTarBase ID miRNA Experiments Reference
MIRT048223 hsa-miR-196a-5p CLASH 23622248
MIRT643548 hsa-miR-4496 HITS-CLIP 23824327
MIRT643547 hsa-miR-4768-3p HITS-CLIP 23824327
MIRT643546 hsa-miR-4459 HITS-CLIP 23824327
MIRT643545 hsa-miR-4433a-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
39
GO ID Ontology Definition Evidence Reference
GO:0000295 Function Adenine nucleotide transmembrane transporter activity TAS
GO:0001561 Process Fatty acid alpha-oxidation TAS
GO:0005347 Function ATP transmembrane transporter activity IBA
GO:0005347 Function ATP transmembrane transporter activity IGI 12445829
GO:0005515 Function Protein binding IPI 10704444, 11402059, 14709540, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606795 10987 ENSG00000100372
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O43808
Protein name Peroxisomal membrane protein PMP34 (34 kDa peroxisomal membrane protein) (Solute carrier family 25 member 17)
Protein function Peroxisomal transporter for multiple cofactors like coenzyme A (CoA), flavin adenine dinucleotide (FAD), flavin mononucleotide (FMN) and nucleotide adenosine monophosphate (AMP), and to a lesser extent for nicotinamide adenine dinucleotide (NAD(
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00153 Mito_carr 6 97 Mitochondrial carrier protein Family
PF00153 Mito_carr 97 197 Mitochondrial carrier protein Family
PF00153 Mito_carr 199 297 Mitochondrial carrier protein Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Expressed in liver. {ECO:0000269|PubMed:22185573, ECO:0000269|PubMed:9874197}.
Sequence
Sequence length 307
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Peroxisome   Alpha-oxidation of phytanate
Class I peroxisomal membrane protein import
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Uveal melanoma Uncertain significance rs144758492 RCV005931026
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Lymphatic Metastasis Associate 37386359
Neoplasms Associate 37386359
Squamous Cell Carcinoma of Head and Neck Associate 37386359