ARL4A

ARF like GTPase 4A P40617 ARL4A_HUMAN
Protein Coding Chr 7 7p21.3 Swiss-Prot reviewed Entrez 10124
Mutations
372
CL 55 · Tissue 315
Samples
73
CL 10 · Tissue 61
Peptides
69
unique mutant peptides
Transcripts
5
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
Mutations37255315
Samples731061
Peptides691158

Function

ARL4A · ARF like GTPase 4A

ADP-ribosylation factor-like 4A is a member of the ADP-ribosylation factor family of GTP-binding proteins. ARL4A is similar to ARL4C and ARL4D and each has a nuclear localization signal and an unusually high guaninine nucleotide exchange rate. ARL4A is located in both the nuclear and extranuclear cell compartments. Multiple transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

5 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
ENST00000396662 P40617 76 69
ENST00000356797 P40617 74 67
ENST00000396663 P40617 74 67
ENST00000396664 P40617 74 67
ENST00000404894 P40617 74 67

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7p21.3
Entrez ID
Aliases
ARL4

Recurrent Mutations

All 69 amino-acid changes on canonical ENST00000396662 · 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 ARL4A · 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 ARL4A – 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
Unknown
0/10 0%
1/29 3%
Endometrial Carcinoma
0/42 0%
8/612 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Squamous Cell Lung Carcinoma
1/57 2%
3/810 0%
Mesothelioma
1/62 2%
0/165 0%
Colorectal Carcinoma
2/143 1%
9/3239 0%
Non-Small Cell Lung Carcinoma
0/304 0%
5/1390 0%
Other Solid Cancers
1/94 1%
3/1515 0%
Melanoma
0/210 0%
5/1899 0%
Gastric Carcinoma
1/74 1%
3/1809 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
B-Lymphoblastic Leukemia
1/55 2%
2/2640 0%
Non-Cancerous
0/104 0%
1/830 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Prostate Carcinoma
0/13 0%
2/2105 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
1/2550 0%
Neuroblastoma
1/87 1%
0/1331 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Glioma
0/52 0%
1/2127 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
0/2534 0%

Mutation Distribution

Where ARL4A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ARL4A 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 372 mutations in ARL4A

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