ABCB9

ATP binding cassette subfamily B member 9 Q9NP78 ABCB9_HUMAN
Protein Coding Chr 12 12q24.31 Swiss-Prot reviewed Entrez 23457
Mutations
1,811
CL 208 · Tissue 1,568
Samples
283
CL 55 · Tissue 222
Peptides
262
unique mutant peptides
Transcripts
7
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
Mutations1,8112081,568
Samples28355222
Peptides26247220

Function

ABCB9 · ATP binding cassette subfamily B member 9

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 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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This family member functions in the translocation of peptides from the cytosol into the lysosomal lumen. Alternative splicing of this gene results in distinct isoforms which are likely to have different substrate specificities. [provided by RefSeq, Jul 2011].

Isoforms & Proteins

7 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
ENST00000280560 Q9NP78 303 244
ENST00000392439 Q9NP78 265 220
ENST00000542678 Q9NP78 265 220
ENST00000346530 Q9NP78-2 257 212
ENST00000540285 Q9NP78-7 247 204
ENST00000344275 Q9NP78-6 237 198
ENST00000442833 Q9NP78-5 237 198

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q24.31
Entrez ID
Aliases
EST122234TAPL

Recurrent Mutations

All 244 amino-acid changes on canonical ENST00000280560 · 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 ABCB9 · 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 ABCB9 – 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
5/40 12%
0/0 0%
Endometrial Carcinoma
2/42 5%
15/612 2%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Melanoma
9/210 4%
34/1899 2%
Colorectal Carcinoma
5/143 4%
46/3239 1%
Other Sarcomas
4/69 6%
4/699 1%
Non-Small Cell Lung Carcinoma
3/304 1%
12/1390 1%
Cervical Carcinoma
1/35 3%
3/422 1%
Thyroid Gland Carcinoma
2/45 4%
12/1592 1%
Other Solid Cancers
3/94 3%
10/1515 1%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Squamous Cell Lung Carcinoma
1/57 2%
5/810 1%
Gastric Carcinoma
2/74 3%
10/1809 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Glioma
4/52 8%
8/2127 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Esophageal Carcinoma
1/23 4%
3/769 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Ovarian Carcinoma
0/109 0%
5/998 0%
Mesothelioma
1/62 2%
0/165 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
10/2550 0%
Neuroendocrine Tumour
0/154 0%
3/577 1%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Non-Cancerous
0/104 0%
3/830 0%
Head and Neck Carcinoma
3/85 4%
2/1574 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Prostate Carcinoma
0/13 0%
5/2105 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
6/2534 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Medulloblastoma
0/0 0%
1/450 0%

Mutation Distribution

Where ABCB9 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ABCB9 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 1,811 mutations in ABCB9

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