ABCA10

ATP binding cassette subfamily A member 10 Q8WWZ4 ABCAA_HUMAN
Protein Coding Chr 17 17q24.3 Swiss-Prot reviewed Entrez 10349
Mutations
859
CL 193 · Tissue 660
Samples
740
CL 167 · Tissue 568
Peptides
612
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
Mutations859193660
Samples740167568
Peptides612126508

Function

ABCA10 · ATP binding cassette subfamily A member 10

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24, but neither the substrate nor the function of this gene is known. [provided by RefSeq, Jul 2008].

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
ENST00000269081 Q8WWZ4 754 576
ENST00000690296 Q8WWZ4 105 97

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q24.3
Entrez ID
Aliases
EST698739

Recurrent Mutations

All 576 amino-acid changes on canonical ENST00000269081 · 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 ABCA10 · 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 ABCA10 – 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
8/40 20%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
7/42 17%
32/612 5%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Non-Small Cell Lung Carcinoma
28/304 9%
45/1390 3%
Glioblastoma
4/98 4%
0/0 0%
Melanoma
9/210 4%
74/1899 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Squamous Cell Lung Carcinoma
2/57 4%
25/810 3%
Other Solid Cancers
4/94 4%
41/1515 3%
Bladder Carcinoma
2/58 3%
25/956 3%
Colorectal Carcinoma
20/143 14%
68/3239 2%
Rhabdomyosarcoma
1/33 3%
4/171 2%
Gastric Carcinoma
3/74 4%
35/1809 2%
Cervical Carcinoma
2/35 6%
6/422 1%
Ovarian Carcinoma
7/109 6%
12/998 1%
Germ Cell Tumour
0/25 0%
3/169 2%
Neuroendocrine Tumour
7/154 5%
4/577 1%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Glioma
2/52 4%
23/2127 1%
Breast Carcinoma
13/144 9%
26/3264 1%
Head and Neck Carcinoma
3/85 4%
14/1574 1%
Biliary Tract Carcinoma
3/54 6%
7/950 1%
Esophageal Squamous Cell Carcinoma
5/51 10%
19/2550 1%
Hepatocellular Carcinoma
3/46 7%
17/2210 1%
Kidney Carcinoma
2/85 2%
14/1862 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
B-Cell Non-Hodgkins Lymphoma
10/88 11%
9/2534 0%

Mutation Distribution

Where ABCA10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ABCA10 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 859 mutations in ABCA10

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