ALS2

Alsin Rho guanine nucleotide exchange factor ALS2 Q96Q42 ALS2_HUMAN
Protein Coding Chr 2 2q33.1 Swiss-Prot reviewed Entrez 57679
Mutations
806
CL 134 · Tissue 652
Samples
616
CL 119 · Tissue 489
Peptides
538
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
Mutations806134652
Samples616119489
Peptides53881449

Function

ALS2 · Alsin Rho guanine nucleotide exchange factor ALS2

The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008].

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
ENST00000264276 Q96Q42 669 529
ENST00000467448 Q96Q42-2 135 113
ENST00000680163 Q96Q42 2 2

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q33.1
Entrez ID
Aliases
ALS2CR6ALSJIAHSPPLSJ

Recurrent Mutations

All 529 amino-acid changes on canonical ENST00000264276 · 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 ALS2 · 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 ALS2 – 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
3/25 12%
0/0 0%
Endometrial Carcinoma
12/42 29%
31/612 5%
Gastrointestinal Stromal Tumour
0/0 0%
7/133 5%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Squamous Cell Lung Carcinoma
5/57 9%
26/810 3%
Melanoma
4/210 2%
64/1899 3%
Colorectal Carcinoma
20/143 14%
72/3239 2%
Non-Small Cell Lung Carcinoma
14/304 5%
31/1390 2%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Glioblastoma
2/98 2%
0/0 0%
Gastric Carcinoma
3/74 4%
35/1809 2%
Cervical Carcinoma
2/35 6%
7/422 2%
Bladder Carcinoma
1/58 2%
16/956 2%
Plasma Cell Myeloma
3/44 7%
2/305 1%
Mesothelioma
2/62 3%
1/165 1%
Hepatocellular Carcinoma
2/46 4%
27/2210 1%
Other Solid Cancers
0/94 0%
20/1515 1%
Small Cell Lung Carcinoma
2/9 22%
7/752 1%
Head and Neck Carcinoma
2/85 2%
17/1574 1%
Chondrosarcoma
0/14 0%
1/75 1%
Neuroendocrine Tumour
3/154 2%
5/577 1%
Breast Carcinoma
12/144 8%
23/3264 1%
Ovarian Carcinoma
1/109 1%
9/998 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Biliary Tract Carcinoma
1/54 2%
7/950 1%
Other Sarcomas
0/69 0%
6/699 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
B-Cell Non-Hodgkins Lymphoma
5/88 6%
13/2534 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
15/2550 1%

Mutation Distribution

Where ALS2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ALS2 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 806 mutations in ALS2

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