HLA-DMB

Major histocompatibility complex, class II, DM beta P28068 DMB_HUMAN
Protein Coding Chr 6 6p21.32 Swiss-Prot reviewed Entrez 3109
Mutations
147
CL 44 · Tissue 102
Samples
140
CL 44 · Tissue 95
Peptides
106
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
Mutations14744102
Samples1404495
Peptides1062979

Function

HLA-DMB · Major histocompatibility complex, class II, DM beta

HLA-DMB belongs to the HLA class II beta chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta (DMB) chain, both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP (class II-associated invariant chain peptide) molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The beta chain is approximately 26-28 kDa and its gene contains 6 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and exon 5 encodes the cytoplasmic tail. [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
ENST00000418107 P28068 147 106

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6p21.32
Entrez ID
Aliases
D6S221ERING7

Recurrent Mutations

All 106 amino-acid changes on canonical ENST00000418107 · 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 HLA-DMB · 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 HLA-DMB – 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
3/40 8%
0/0 0%
Melanoma
3/210 1%
23/1899 1%
Cervical Carcinoma
2/35 6%
3/422 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Osteosarcoma
1/45 2%
0/166 0%
Squamous Cell Lung Carcinoma
4/57 7%
0/810 0%
Endometrial Carcinoma
1/42 2%
2/612 0%
Colorectal Carcinoma
4/143 3%
11/3239 0%
B-Cell Non-Hodgkins Lymphoma
6/88 7%
3/2534 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Glioma
1/52 2%
5/2127 0%
Prostate Carcinoma
2/13 15%
4/2105 0%
Ovarian Carcinoma
3/109 3%
0/998 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Other Sarcomas
2/69 3%
0/699 0%
Other Blood Cancers
2/61 3%
5/2725 0%
Non-Small Cell Lung Carcinoma
1/304 0%
3/1390 0%
Head and Neck Carcinoma
2/85 2%
2/1574 0%
Medulloblastoma
0/0 0%
1/450 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
Breast Carcinoma
1/144 1%
4/3264 0%
Kidney Carcinoma
1/85 1%
2/1862 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
1/2550 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%

Mutation Distribution

Where HLA-DMB is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HLA-DMB 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 147 mutations in HLA-DMB

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