H3C4

H3 clustered histone 4 P68431 H31_HUMAN
Protein Coding Chr 6 6p22.2 Swiss-Prot reviewed Entrez 8351
Mutations
20
CL 9 · Tissue 0
Samples
16
CL 9 · Tissue 0
Peptides
20
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
Mutations2090
Samples1690
Peptides2090

Function

H3C4 · H3 clustered histone 4

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H3 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015].

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
ENST00000356476 P68431 20 20

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6p22.2
Entrez ID
Aliases
H3/bH3FBHIST1H3D

Recurrent Mutations

All 20 amino-acid changes on canonical ENST00000356476 · 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 H3C4 · 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 H3C4 – 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
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Endometrial Carcinoma
1/42 2%
1/612 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Non-Small Cell Lung Carcinoma
1/304 0%
1/1390 0%
Melanoma
1/210 0%
1/1899 0%
Colorectal Carcinoma
1/143 1%
1/3239 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
0/2550 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
0/2534 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where H3C4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in H3C4 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.

Mutations

All 20 mutations in H3C4

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