HSP90B1

Heat shock protein 90 beta family member 1 P14625 ENPL_HUMAN
Protein Coding Chr 12 12q23.3 Swiss-Prot reviewed Entrez 7184
Mutations
423
CL 52 · Tissue 362
Samples
307
CL 47 · Tissue 253
Peptides
247
unique mutant peptides
Transcripts
3
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
Mutations42352362
Samples30747253
Peptides24730217

Function

HSP90B1 · Heat shock protein 90 beta family member 1

This gene encodes a member of a family of adenosine triphosphate(ATP)-metabolizing molecular chaperones with roles in stabilizing and folding other proteins. The encoded protein is localized to melanosomes and the endoplasmic reticulum. Expression of this protein is associated with a variety of pathogenic states, including tumor formation. There is a microRNA gene located within the 5' exon of this gene. There are pseudogenes for this gene on chromosomes 1 and 15. [provided by RefSeq, Aug 2012].

Isoforms & Proteins

3 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
ENST00000299767 P14625 323 245
ENST00000614327 A0A087WT78* 98 83
ENST00000681861 A0A7P0TAT8* 2 2

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q23.3
Entrez ID
Aliases
ECGPGP96GRP94HEL-S-125mHEL35TRA1

Recurrent Mutations

All 245 amino-acid changes on canonical ENST00000299767 · 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 HSP90B1 · 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 HSP90B1 – 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
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
5/42 12%
18/612 3%
Glioblastoma
3/98 3%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Cervical Carcinoma
4/35 11%
4/422 1%
Bladder Carcinoma
0/58 0%
15/956 2%
Colorectal Carcinoma
7/143 5%
42/3239 1%
Non-Small Cell Lung Carcinoma
4/304 1%
17/1390 1%
Melanoma
2/210 1%
21/1899 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
26/2550 1%
Ewings Sarcoma
2/63 3%
1/262 0%
Mesothelioma
2/62 3%
0/165 0%
Burkitts Lymphoma
0/32 0%
2/196 1%
Hepatocellular Carcinoma
0/46 0%
19/2210 1%
Other Sarcomas
2/69 3%
4/699 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Head and Neck Carcinoma
3/85 4%
9/1574 1%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Gastric Carcinoma
0/74 0%
9/1809 0%
Osteosarcoma
0/45 0%
1/166 1%
Medulloblastoma
0/0 0%
2/450 0%
Thyroid Gland Carcinoma
0/45 0%
7/1592 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Glioma
0/52 0%
8/2127 0%
Breast Carcinoma
5/144 3%
7/3264 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%

Mutation Distribution

Where HSP90B1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in HSP90B1 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 423 mutations in HSP90B1

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