ABCD4

ATP binding cassette subfamily D member 4 O14678 ABCD4_HUMAN
Protein Coding Chr 14 14q24.3 Swiss-Prot reviewed Entrez 5826
Mutations
438
CL 92 · Tissue 338
Samples
315
CL 75 · Tissue 235
Peptides
241
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
Mutations43892338
Samples31575235
Peptides24158194

Function

ABCD4 · ATP binding cassette subfamily D member 4

The 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 intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. The function of this peroxisomal membrane protein is unknown. However, it is speculated that it may function as a heterodimer for another peroxisomal ABC transporter and, therefore, may modify the adrenoleukodystrophy phenotype. It may also play a role in the process of peroxisome biogenesis. Alternative splicing results in several protein-coding and non-protein-coding variants. [provided by RefSeq, Jul 2017].

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
ENST00000356924 O14678 336 232
ENST00000557588 G3V4U7* 102 76

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q24.3
Entrez ID
Aliases
ABC41EST352188MAHCJP70RP79RPMP69

Recurrent Mutations

All 232 amino-acid changes on canonical ENST00000356924 · 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 ABCD4 · 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 ABCD4 – 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
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Endometrial Carcinoma
4/42 10%
11/612 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Melanoma
4/210 2%
33/1899 2%
Non-Small Cell Lung Carcinoma
12/304 4%
14/1390 1%
Other Solid Cancers
4/94 4%
18/1515 1%
Cervical Carcinoma
0/35 0%
6/422 1%
Colorectal Carcinoma
8/143 6%
35/3239 1%
Gastric Carcinoma
5/74 7%
18/1809 1%
Head and Neck Carcinoma
2/85 2%
13/1574 1%
Bladder Carcinoma
2/58 3%
7/956 1%
Burkitts Lymphoma
0/32 0%
2/196 1%
Non-Cancerous
1/104 1%
7/830 1%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Squamous Cell Lung Carcinoma
3/57 5%
4/810 0%
Glioma
0/52 0%
11/2127 1%
Osteosarcoma
1/45 2%
0/166 0%
Kidney Carcinoma
3/85 4%
6/1862 0%
Hepatocellular Carcinoma
2/46 4%
8/2210 0%
Neuroendocrine Tumour
1/154 1%
2/577 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Ovarian Carcinoma
2/109 2%
2/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
9/2550 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Thyroid Gland Carcinoma
2/45 4%
3/1592 0%
Other Sarcomas
0/69 0%
2/699 0%
Breast Carcinoma
5/144 3%
4/3264 0%
Esophageal Carcinoma
0/23 0%
2/769 0%

Mutation Distribution

Where ABCD4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ABCD4 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 438 mutations in ABCD4

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