ALMS1

ALMS1 centrosome and basal body associated protein Q8TCU4 ALMS1_HUMAN
Protein Coding Chr 2 2p13.1 Swiss-Prot reviewed Entrez 7840
Mutations
5,428
CL 805 · Tissue 4,572
Samples
1,649
CL 356 · Tissue 1,275
Peptides
1,451
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
Mutations5,4288054,572
Samples1,6493561,275
Peptides1,4512471,216

Function

ALMS1 · ALMS1 centrosome and basal body associated protein

This gene encodes a protein containing a large tandem-repeat domain as well as additional low complexity regions. The encoded protein functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations in this gene cause Alstrom syndrome. There is a pseudogene for this gene located adjacent in the same region of chromosome 2. Alternative splice variants have been described but their full length nature has not been determined. [provided by RefSeq, Apr 2014].

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
ENST00000613296 Q8TCU4 2,018 1,436
ENST00000484298 A0A087WTU9* 1,792 1,350
ENST00000614410 A0A087WV20* 1,618 1,235

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p13.1
Entrez ID
Aliases
ALSS

Recurrent Mutations

All 1436 amino-acid changes on canonical ENST00000613296 · 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 ALMS1 · 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 ALMS1 – 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
T-Lymphoblastic Leukemia
11/40 28%
0/0 0%
Chronic Myelogenous Leukemia
5/25 20%
0/0 0%
Endometrial Carcinoma
15/42 36%
55/612 9%
Acute Myeloid Leukemia
9/90 10%
0/0 0%
Melanoma
28/210 13%
177/1899 9%
Oral Cavity Carcinoma
5/54 9%
0/0 0%
Other Solid Cancers
13/94 14%
121/1515 8%
Glioblastoma
8/98 8%
0/0 0%
Non-Small Cell Lung Carcinoma
52/304 17%
80/1390 6%
T-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
Squamous Cell Lung Carcinoma
8/57 14%
52/810 6%
Gastric Carcinoma
11/74 15%
98/1809 5%
Bladder Carcinoma
7/58 12%
49/956 5%
Neuroendocrine Tumour
21/154 14%
19/577 3%
Gastrointestinal Stromal Tumour
0/0 0%
7/133 5%
Cervical Carcinoma
7/35 20%
17/422 4%
Colorectal Carcinoma
25/143 17%
142/3239 4%
Chondrosarcoma
2/14 14%
2/75 3%
Small Cell Lung Carcinoma
4/9 44%
29/752 4%
Rhabdomyosarcoma
1/33 3%
7/171 4%
Hodgkins Lymphoma
4/16 25%
1/122 1%
Esophageal Carcinoma
1/23 4%
20/769 3%
Esophageal Squamous Cell Carcinoma
8/51 16%
59/2550 2%
Hepatocellular Carcinoma
7/46 15%
51/2210 2%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Unknown
1/10 10%
0/29 0%
Ovarian Carcinoma
13/109 12%
15/998 2%
Biliary Tract Carcinoma
4/54 7%
18/950 2%
Other Sarcomas
6/69 9%
10/699 1%
Germ Cell Tumour
2/25 8%
2/169 1%

Mutation Distribution

Where ALMS1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ALMS1 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 5,428 mutations in ALMS1

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