KIAA2026

Uncharacterized bromodomain-containing protein 10 Q5HYC2 BRD10_HUMAN
Swiss-Prot reviewed
Mutations
1,430
CL 201 · Tissue 1,163
Samples
590
CL 80 · Tissue 504
Peptides
597
unique mutant peptides
Transcripts
2
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
Mutations1,4302011,163
Samples59080504
Peptides59782502

Isoforms & Proteins

2 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
ENST00000399933 Q5HYC2 721 585
ENST00000381461 Q5HYC2-2 709 580

Gene Properties

Recurrent Mutations

All 585 amino-acid changes on canonical ENST00000399933 · 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 KIAA2026 · 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 KIAA2026 – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
2/42 5%
42/612 7%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Cervical Carcinoma
0/35 0%
15/422 4%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Melanoma
5/210 2%
47/1899 2%
Colorectal Carcinoma
9/143 6%
68/3239 2%
Other Solid Cancers
3/94 3%
32/1515 2%
Bladder Carcinoma
0/58 0%
22/956 2%
Squamous Cell Lung Carcinoma
2/57 4%
16/810 2%
Glioblastoma
2/98 2%
0/0 0%
Non-Small Cell Lung Carcinoma
8/304 3%
25/1390 2%
Gastric Carcinoma
4/74 5%
27/1809 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Neuroendocrine Tumour
5/154 3%
4/577 1%
Head and Neck Carcinoma
1/85 1%
19/1574 1%
Small Cell Lung Carcinoma
0/9 0%
9/752 1%
Ovarian Carcinoma
4/109 4%
9/998 1%
Chondrosarcoma
1/14 7%
0/75 0%
Other Sarcomas
1/69 1%
7/699 1%
Breast Carcinoma
3/144 2%
32/3264 1%
Biliary Tract Carcinoma
0/54 0%
10/950 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Non-Cancerous
0/104 0%
9/830 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Glioma
0/52 0%
19/2127 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%

Mutation Distribution

Where KIAA2026 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KIAA2026 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 1,430 mutations in KIAA2026

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