Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10478
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 25 member 17
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC25A17
Synonyms (NCBI Gene) Gene synonyms aliases
PMP34
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q13.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 21873635
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606795 10987 ENSG00000100372
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Bipolar Disorder Bipolar Disorder GWAS
Neuroticism Neuroticism GWAS
Colorectal Cancer Colorectal Cancer In summary, our data strongly demonstrated that upregulation of GRB7 conferred MEKi resistance in CRC cells with KRAS mutations by mediating RTK signaling through the recruitment of PLK1. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Lymphatic Metastasis Associate 37386359
Neoplasms Associate 37386359
Squamous Cell Carcinoma of Head and Neck Associate 37386359