Gene Gene information from NCBI Gene database.
Entrez ID 25874
Gene name Mitochondrial pyruvate carrier 2
Gene symbol MPC2
Synonyms (NCBI Gene)
BRP44SLC54A2
Chromosome 1
Chromosome location 1q24.2
miRNA miRNA information provided by mirtarbase database.
1
miRTarBase ID miRNA Experiments Reference
MIRT030303 hsa-miR-26b-5p Microarray 19088304
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 31145700, 32296183, 32814053, 33961781, 35278701
GO:0005634 Component Nucleus HDA 21630459
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IDA
GO:0005739 Component Mitochondrion IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614737 24515 ENSG00000143158
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95563
Protein name Mitochondrial pyruvate carrier 2 (Brain protein 44)
Protein function Mediates the uptake of pyruvate into mitochondria.
PDB 8YW6 , 8YW8 , 8YW9 , 9KNW , 9KNX , 9KNY , 9MNW , 9MNX , 9MNY , 9MNZ , 9MO0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03650 MPC 27 127 Mitochondrial pyruvate carriers Family
Sequence
Sequence length 127
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Diabetic cardiomyopathy  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
METABOLIC DISEASE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
METABOLIC DISEASES Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
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
Diabetic Nephropathies Diabetic neuropathy Pubtator 32664896 Inhibit
★☆☆☆☆
Found in Text Mining only
Familial lichen amyloidosis Lichen amyloidosis BEFREE 27852261
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 29547090
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 29547090
★☆☆☆☆
Found in Text Mining only
Glioma Glioma BEFREE 29547090
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 35242216 Associate
★☆☆☆☆
Found in Text Mining only
Leukemia, Myelocytic, Acute Leukemia GWASCAT_DG 27903959
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 29805642
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Lymphatic metastasis Pubtator 27852261 Associate
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of prostate Prostate cancer BEFREE 27852261
★☆☆☆☆
Found in Text Mining only