BCKDHA (branched chain keto acid dehydrogenase E1 subunit alpha)

2014-11-01  

Identity

HGNC
LOCATION
19q13.2
LOCUSID
ALIAS
BCKDE1A,MSU,MSUD1,OVD1A
FUSION GENES

Other Information

Locus ID:

NCBI: 593
MIM: 608348
HGNC: 986
Ensembl: ENSG00000248098

Variants:

dbSNP: 593
ClinVar: 593
TCGA: ENSG00000248098
COSMIC: BCKDHA

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000248098ENST00000269980P12694
ENSG00000248098ENST00000269980A0A024R0K3
ENSG00000248098ENST00000457836P12694
ENSG00000248098ENST00000541315H0YH31
ENSG00000248098ENST00000542943F5GXU9
ENSG00000248098ENST00000544905H0YH20

Expression (GTEx)

0
10
20
30
40
50
60
70
80
90
100

Pathways

PathwaySourceExternal ID
Valine, leucine and isoleucine degradationKEGGko00280
Propanoate metabolismKEGGko00640
Valine, leucine and isoleucine degradationKEGGhsa00280
Propanoate metabolismKEGGhsa00640
Metabolic pathwaysKEGGhsa01100
Leucine degradation, leucine => acetoacetate + acetyl-CoAKEGGhsa_M00036
Leucine degradation, leucine => acetoacetate + acetyl-CoAKEGGM00036
MetabolismREACTOMER-HSA-1430728
Metabolism of amino acids and derivativesREACTOMER-HSA-71291
Branched-chain amino acid catabolismREACTOMER-HSA-70895
Glyoxylate metabolism and glycine degradationREACTOMER-HSA-389661

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
348830032022Three novel mutations of the BCKDHA, BCKDHB and DBT genes in Chinese children with maple syrup urine disease.0
348830032022Three novel mutations of the BCKDHA, BCKDHB and DBT genes in Chinese children with maple syrup urine disease.0
345112902021Association of BCAT2 and BCKDH polymorphisms with clinical, anthropometric and biochemical parameters in young adults.2
345112902021Association of BCAT2 and BCKDH polymorphisms with clinical, anthropometric and biochemical parameters in young adults.2
293069282018Four novel mutations of the BCKDHA, BCKDHB and DBT genes in Iranian patients with maple syrup urine disease.2
293070172018Clinical characteristics and mutation analysis of five Chinese patients with maple syrup urine disease.5
296735822018In silico prediction of the pathogenic effect of a novel variant of BCKDHA leading to classical maple syrup urine disease identified using clinical exome sequencing.0
293069282018Four novel mutations of the BCKDHA, BCKDHB and DBT genes in Iranian patients with maple syrup urine disease.2
293070172018Clinical characteristics and mutation analysis of five Chinese patients with maple syrup urine disease.5
296735822018In silico prediction of the pathogenic effect of a novel variant of BCKDHA leading to classical maple syrup urine disease identified using clinical exome sequencing.0
268307102016Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias.3
268307102016Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias.3
264538402015Eleven novel mutations of the BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease in the Chinese population: Report on eight cases.6
264538402015Eleven novel mutations of the BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease in the Chinese population: Report on eight cases.6
242688122014Different gene preferences of maple syrup urine disease in the aboriginal tribes of Taiwan.1

Citation

Dessen P

BCKDHA (branched chain keto acid dehydrogenase E1 subunit alpha)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/60724/img/gene-explorer/haematological-explorer/