ABCB5

ATP binding cassette subfamily B member 5 Q2M3G0 ABCB5_HUMAN
Protein Coding Chr 7 7p21.1 Swiss-Prot reviewed Entrez 340273
Mutations
2,341
CL 352 · Tissue 1,970
Samples
1,128
CL 211 · Tissue 904
Peptides
828
unique mutant peptides
Transcripts
4
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
Mutations2,3413521,970
Samples1,128211904
Peptides828140718

Function

ABCB5 · ATP binding cassette subfamily B member 5

ABCB5 belongs to the ATP-binding cassette (ABC) transporter superfamily of integral membrane proteins. These proteins participate in ATP-dependent transmembrane transport of structurally diverse molecules ranging from small ions, sugars, and peptides to more complex organic molecules (Chen et al., 2005 [PubMed 15760339]).[supplied by OMIM, Mar 2008].

Isoforms & Proteins

4 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
ENST00000404938 Q2M3G0 1,288 786
ENST00000258738 Q2M3G0-1 799 509
ENST00000443026 Q2M3G0-2 133 87
ENST00000406935 Q2M3G0-3 121 81

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7p21.1
Entrez ID
Aliases
ABCB5alphaABCB5betaEST422562

Recurrent Mutations

All 786 amino-acid changes on canonical ENST00000404938 · 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 ABCB5 · 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 ABCB5 – 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
11/40 28%
0/0 0%
Oral Cavity Carcinoma
5/54 9%
0/0 0%
Melanoma
11/210 5%
170/1899 9%
T-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
Non-Small Cell Lung Carcinoma
42/304 14%
78/1390 6%
Endometrial Carcinoma
7/42 17%
35/612 6%
Squamous Cell Lung Carcinoma
9/57 16%
41/810 5%
Rhabdomyosarcoma
0/33 0%
11/171 6%
Gastrointestinal Stromal Tumour
0/0 0%
7/133 5%
Hodgkins Lymphoma
2/16 12%
4/122 3%
Glioblastoma
4/98 4%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Neuroendocrine Tumour
16/154 10%
10/577 2%
Gastric Carcinoma
10/74 14%
54/1809 3%
Other Solid Cancers
1/94 1%
52/1515 3%
Colorectal Carcinoma
20/143 14%
82/3239 3%
Bladder Carcinoma
3/58 5%
27/956 3%
Esophageal Squamous Cell Carcinoma
9/51 18%
63/2550 2%
Cervical Carcinoma
2/35 6%
10/422 2%
Unknown
0/10 0%
1/29 3%
Small Cell Lung Carcinoma
0/9 0%
19/752 3%
Other Sarcomas
9/69 13%
10/699 1%
Non-Cancerous
11/104 11%
7/830 1%
Hepatocellular Carcinoma
1/46 2%
42/2210 2%
Esophageal Carcinoma
0/23 0%
14/769 2%
Adrenocortical Carcinoma
0/3 0%
2/112 2%
Plasma Cell Myeloma
4/44 9%
2/305 1%
Germ Cell Tumour
1/25 4%
2/169 1%
Biliary Tract Carcinoma
2/54 4%
13/950 1%
Osteosarcoma
2/45 4%
1/166 1%

Mutation Distribution

Where ABCB5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ABCB5 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 38 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 2,341 mutations in ABCB5

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