DNAL4

Dynein axonemal light chain 4 O96015 DNAL4_HUMAN
Protein Coding Chr 22 22q13.1 Swiss-Prot reviewed Entrez 10126
Mutations
77
CL 15 · Tissue 62
Samples
50
CL 11 · Tissue 39
Peptides
41
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
Mutations771562
Samples501139
Peptides41935

Function

DNAL4 · Dynein axonemal light chain 4

This gene encodes an axonemal dynein light chain which functions as a component of the outer dynein arms complex. This complex acts as the molecular motor that provides the force to move cilia in an ATP-dependent manner. The encoded protein is expressed in tissues with motile cilia or flagella and may be involved in the movement of sperm flagella. [provided by RefSeq, Dec 2014].

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
ENST00000216068 O96015 44 32
ENST00000406199 B0QXZ5* 33 26

Gene Properties

Type
Protein Coding
Chromosome
22
Cytoband
22q13.1
Entrez ID
Aliases
MRMV3PIG27

Recurrent Mutations

All 32 amino-acid changes on canonical ENST00000216068 · 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 DNAL4 · 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 DNAL4 – 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
Cervical Carcinoma
2/35 6%
2/422 0%
Squamous Cell Lung Carcinoma
1/57 2%
3/810 0%
Mesothelioma
1/62 2%
0/165 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Bladder Carcinoma
2/58 3%
1/956 0%
Non-Small Cell Lung Carcinoma
0/304 0%
5/1390 0%
Melanoma
1/210 0%
4/1899 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Gastric Carcinoma
1/74 1%
3/1809 0%
Colorectal Carcinoma
3/143 2%
4/3239 0%
Endometrial Carcinoma
0/42 0%
1/612 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Other Blood Cancers
0/61 0%
3/2725 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where DNAL4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DNAL4 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 77 mutations in DNAL4

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