LAMA2

Laminin subunit alpha 2 P24043 LAMA2_HUMAN
Protein Coding Chr 6 6q22.33 Swiss-Prot reviewed Entrez 3908
Mutations
5,274
CL 746 · Tissue 4,468
Samples
1,857
CL 331 · Tissue 1,504
Peptides
1,746
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
Mutations5,2747464,468
Samples1,8573311,504
Peptides1,7462761,498

Function

LAMA2 · Laminin subunit alpha 2

Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Jul 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
ENST00000421865 P24043 2,353 1,640
ENST00000617695 A0A087WYF1* 2,089 1,551
ENST00000618192 A0A087WX80* 832 636

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6q22.33
Entrez ID
Aliases
LAMMMDC1A

Recurrent Mutations

All 1640 amino-acid changes on canonical ENST00000421865 · 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 LAMA2 · 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 LAMA2 – 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
10/40 25%
0/0 0%
Chronic Myelogenous Leukemia
5/25 20%
0/0 0%
Endometrial Carcinoma
13/42 31%
73/612 12%
Melanoma
23/210 11%
224/1899 12%
Non-Small Cell Lung Carcinoma
45/304 15%
131/1390 9%
Squamous Cell Lung Carcinoma
10/57 18%
73/810 9%
Glioblastoma
9/98 9%
0/0 0%
Small Cell Lung Carcinoma
2/9 22%
52/752 7%
Acute Myeloid Leukemia
6/90 7%
0/0 0%
Other Solid Cancers
12/94 13%
94/1515 6%
Neuroendocrine Tumour
28/154 18%
17/577 3%
Colorectal Carcinoma
42/143 29%
161/3239 5%
Gastric Carcinoma
5/74 7%
83/1809 5%
Cervical Carcinoma
3/35 9%
17/422 4%
Bladder Carcinoma
3/58 5%
39/956 4%
Head and Neck Carcinoma
7/85 8%
57/1574 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Plasma Cell Myeloma
8/44 18%
5/305 2%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Esophageal Carcinoma
3/23 13%
26/769 3%
Hodgkins Lymphoma
1/16 6%
4/122 3%
Ewings Sarcoma
5/63 8%
6/262 2%
Hepatocellular Carcinoma
5/46 11%
71/2210 3%
Biliary Tract Carcinoma
4/54 7%
25/950 3%
Esophageal Squamous Cell Carcinoma
6/51 12%
69/2550 3%
Ovarian Carcinoma
3/109 3%
24/998 2%
Non-Cancerous
3/104 3%
19/830 2%
Other Sarcomas
2/69 3%
16/699 2%
Breast Carcinoma
14/144 10%
65/3264 2%

Mutation Distribution

Where LAMA2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LAMA2 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 5,274 mutations in LAMA2

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