HLA-DRB1

Major histocompatibility complex, class II, DR beta 1 P01911 DRB1_HUMAN
Protein Coding Chr 6 6p21.32 Swiss-Prot reviewed Entrez 3123
Mutations
1,019
CL 386 · Tissue 627
Samples
704
CL 346 · Tissue 353
Peptides
180
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
Mutations1,019386627
Samples704346353
Peptides18032150

Function

HLA-DRB1 · Major histocompatibility complex, class II, DR beta 1

HLA-DRB1 belongs to the HLA class II beta chain paralogs. The class II molecule is a heterodimer consisting of an alpha (DRA) and a beta chain (DRB), both anchored in the membrane. It plays a central role in the immune system by presenting peptides derived from extracellular proteins. Class II molecules are expressed in antigen presenting cells. The beta chain is approximately 26-28 kDa. It is encoded by 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. Within the DR molecule the beta chain contains all the polymorphisms specifying the peptide binding specificities. Hundreds of DRB1 alleles have been described and some alleles have increased frequencies associated with certain diseases or conditions. For example, DRB1*1302 has been related to acute and chronic hepatitis B virus persistence. There are multiple pseudogenes of this gene. [provided by RefSeq, Jul 2020].

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
ENST00000360004 P01911 1,019 180

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6p21.32
Entrez ID
Aliases
DRB1HLA-DR1BHLA-DRBSS1

Recurrent Mutations

All 180 amino-acid changes on canonical ENST00000360004 · 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-DRB1 · 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-DRB1 – 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
4/25 16%
0/0 0%
Oral Cavity Carcinoma
6/54 11%
0/0 0%
Glioblastoma
9/98 9%
0/0 0%
Acute Myeloid Leukemia
7/90 8%
0/0 0%
Mesothelioma
10/62 16%
1/165 1%
Rhabdomyosarcoma
2/33 6%
6/171 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Hodgkins Lymphoma
5/16 31%
0/122 0%
Burkitts Lymphoma
8/32 25%
0/196 0%
Osteosarcoma
6/45 13%
1/166 1%
Neuroendocrine Tumour
21/154 14%
2/577 0%
Thyroid Gland Carcinoma
6/45 13%
43/1592 3%
Other Solid Cancers
9/94 10%
33/1515 2%
Unknown
1/10 10%
0/29 0%
Plasma Cell Myeloma
5/44 11%
3/305 1%
Bladder Carcinoma
6/58 10%
17/956 2%
Colorectal Carcinoma
14/143 10%
56/3239 2%
Ovarian Carcinoma
17/109 16%
5/998 0%
Ewings Sarcoma
6/63 10%
0/262 0%
Endometrial Carcinoma
8/42 19%
4/612 1%
Biliary Tract Carcinoma
8/54 15%
9/950 1%
Non-Small Cell Lung Carcinoma
24/304 8%
4/1390 0%
Melanoma
18/210 9%
15/1899 1%
Germ Cell Tumour
3/25 12%
0/169 0%
Cervical Carcinoma
4/35 11%
3/422 1%
Other Blood Cancers
6/61 10%
34/2725 1%
Other Sarcomas
6/69 9%
5/699 1%
Kidney Carcinoma
15/85 18%
11/1862 1%
Squamous Cell Lung Carcinoma
4/57 7%
6/810 1%

Mutation Distribution

Where HLA-DRB1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HLA-DRB1 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 1,019 mutations in HLA-DRB1

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