ACACA

Acetyl-CoA carboxylase alpha Q13085-4 ACACA_HUMAN
Protein Coding Chr 17 17q12 Swiss-Prot reviewed Entrez 31
Mutations
198
CL 100 · Tissue 0
Samples
101
CL 85 · Tissue 0
Peptides
193
unique mutant peptides
Transcripts
1
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
Mutations1981000
Samples101850
Peptides193950

Function

ACACA · Acetyl-CoA carboxylase alpha

Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. There are two ACC forms, alpha and beta, encoded by two different genes. ACC-alpha is highly enriched in lipogenic tissues. The enzyme is under long term control at the transcriptional and translational levels and under short term regulation by the phosphorylation/dephosphorylation of targeted serine residues and by allosteric transformation by citrate or palmitoyl-CoA. Multiple alternatively spliced transcript variants divergent in the 5' sequence and encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000616317 Q13085-4 198 193

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q12
Entrez ID
Aliases
ACACACACADACACalphaACCACC1ACCA

Recurrent Mutations

All 193 amino-acid changes on canonical ENST00000616317 · 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 ACACA · 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 ACACA – 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
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Glioblastoma
2/98 2%
0/0 0%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Non-Small Cell Lung Carcinoma
11/304 4%
2/1390 0%
Neuroendocrine Tumour
5/154 3%
0/577 0%
Endometrial Carcinoma
3/42 7%
1/612 0%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Osteosarcoma
1/45 2%
0/166 0%
Colorectal Carcinoma
14/143 10%
2/3239 0%
Melanoma
8/210 4%
2/1899 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Ovarian Carcinoma
3/109 3%
1/998 0%
Bladder Carcinoma
2/58 3%
1/956 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Other Sarcomas
2/69 3%
0/699 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Biliary Tract Carcinoma
2/54 4%
0/950 0%
Gastric Carcinoma
2/74 3%
1/1809 0%
Small Cell Lung Carcinoma
1/9 11%
0/752 0%
Other Solid Cancers
2/94 2%
0/1515 0%
Head and Neck Carcinoma
1/85 1%
1/1574 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
0/2534 0%
Non-Cancerous
1/104 1%
0/830 0%
Kidney Carcinoma
2/85 2%
0/1862 0%
Breast Carcinoma
2/144 1%
1/3264 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ACACA 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 198 mutations in ACACA

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