Gene Gene information from NCBI Gene database.
Entrez ID 587
Gene name Branched chain amino acid transaminase 2
Gene symbol BCAT2
Synonyms (NCBI Gene)
BCAMBCATMBCT2HVLIPP18
Chromosome 19
Chromosome location 19q13.33
Summary This gene encodes a branched chain aminotransferase found in mitochondria. The encoded protein forms a dimer that catalyzes the first step in the production of the branched chain amino acids leucine, isoleucine, and valine. Multiple transcript variants en
miRNA miRNA information provided by mirtarbase database.
143
miRTarBase ID miRNA Experiments Reference
MIRT028382 hsa-miR-32-5p Sequencing 20371350
MIRT041917 hsa-miR-484 CLASH 23622248
MIRT040021 hsa-miR-615-3p CLASH 23622248
MIRT728218 hsa-miR-92a-3p HITS-CLIP 22473208
MIRT728217 hsa-miR-92b-3p HITS-CLIP 22473208
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
GO ID Ontology Definition Evidence Reference
GO:0003824 Function Catalytic activity IEA
GO:0004084 Function Branched-chain-amino-acid transaminase activity IBA
GO:0004084 Function Branched-chain-amino-acid transaminase activity IEA
GO:0004084 Function Branched-chain-amino-acid transaminase activity TAS 9165094
GO:0005515 Function Protein binding IPI 28514442, 29568061, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
113530 977 ENSG00000105552
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O15382
Protein name Branched-chain-amino-acid aminotransferase, mitochondrial (BCAT(m)) (EC 2.6.1.42) (Placental protein 18) (PP18)
Protein function Catalyzes the first reaction in the catabolism of the essential branched chain amino acids leucine, isoleucine, and valine (PubMed:17050531, PubMed:25653144, PubMed:8702755). May also function as a transporter of branched chain alpha-keto acids
PDB 1EKF , 1EKP , 1EKV , 1KT8 , 1KTA , 2A1H , 2HDK , 2HG8 , 2HGW , 2HGX , 2HHF , 5BWR , 5BWT , 5BWU , 5BWV , 5BWW , 5BWX , 5CR5 , 5HNE , 5I5S , 5I5T , 5I5U , 5I5V , 5I5W , 5I5X , 5I5Y , 5I60 , 5MPR , 6PRX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01063 Aminotran_4 100 350 Amino-transferase class IV Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:11170829}.
Sequence
Sequence length 392
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
8
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Hypervalinemia and hyperleucine-isoleucinemia Pathogenic rs753659619, rs749866079, rs767653663 RCV004774729
RCV001078195
RCV001078196
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
BCAT2-related disorder Likely benign rs140856269, rs368707614 RCV003923763
RCV003916561
Familial prostate cancer - rs2122664642 RCV005930074
Sarcoma Benign rs781275517 RCV005930555
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 28798381
Cholangiocarcinoma Associate 37076565
Diabetic Retinopathy Associate 37522124
Glioblastoma Associate 27932423, 30016590
Leukemia Prolymphocytic T Cell Associate 10086798
Melanoma Stimulate 37801083
Nasopharyngeal Carcinoma Associate 40083932
Neoplasm Metastasis Associate 37801083
Neoplasms Associate 37801083, 39375392, 40005214