BCKDHA

Branched chain keto acid dehydrogenase E1 subunit alpha P12694 ODBA_HUMAN
Protein Coding Chr 19 19q13.2 Swiss-Prot reviewed Entrez 593
Mutations
447
CL 83 · Tissue 358
Samples
230
CL 50 · Tissue 177
Peptides
177
unique mutant peptides
Transcripts
2
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations44783358
Samples23050177
Peptides17738148

Function

BCKDHA · Branched chain keto acid dehydrogenase E1 subunit alpha

The branched-chain alpha-keto acid (BCAA) dehydrogenase (BCKD) complex is an innter mitochondrial enzyme complex that catalyzes the second major step in the catabolism of the branched-chain amino acids leucine, isoleucine, and valine. The BCKD complex consists of three catalytic components: a heterotetrameric (alpha2-beta2) branched-chain alpha-keto acid decarboxylase (E1), a dihydrolipoyl transacylase (E2), and a dihydrolipoamide dehydrogenase (E3). This gene encodes the alpha subunit of the decarboxylase (E1) component. Mutations in this gene result in maple syrup urine disease, type IA. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009].

Isoforms & Proteins

2 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000269980 P12694 239 158
ENST00000457836 P12694-2 208 141

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.2
Entrez ID
Aliases
BCKDE1AMSUMSUD1MSUD1AOVD1A

Recurrent Mutations

All 158 amino-acid changes on canonical ENST00000269980 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in BCKDHA · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in BCKDHA – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
Endometrial Carcinoma
2/42 5%
9/612 1%
Germ Cell Tumour
2/25 8%
1/169 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Colorectal Carcinoma
6/143 4%
34/3239 1%
Non-Small Cell Lung Carcinoma
11/304 4%
7/1390 0%
Melanoma
7/210 3%
15/1899 1%
Gastric Carcinoma
1/74 1%
17/1809 1%
Burkitts Lymphoma
1/32 3%
1/196 1%
Squamous Cell Lung Carcinoma
2/57 4%
5/810 1%
Bladder Carcinoma
0/58 0%
7/956 1%
Neuroendocrine Tumour
2/154 1%
3/577 1%
Other Sarcomas
0/69 0%
5/699 1%
Thyroid Gland Carcinoma
2/45 4%
8/1592 0%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Ovarian Carcinoma
1/109 1%
4/998 0%
Other Solid Cancers
0/94 0%
7/1515 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Non-Cancerous
0/104 0%
4/830 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
10/2550 0%
Kidney Carcinoma
1/85 1%
5/1862 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Prostate Carcinoma
0/13 0%
5/2105 0%
Medulloblastoma
0/0 0%
1/450 0%
Wilms Tumour
0/5 0%
1/474 0%
Breast Carcinoma
0/144 0%
6/3264 0%

Mutation Distribution

Where BCKDHA is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in BCKDHA were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 447 mutations in BCKDHA

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide