LIMA1

LIM domain and actin binding 1 Q9UHB6 LIMA1_HUMAN
Protein Coding Chr 12 12q13.12 Swiss-Prot reviewed Entrez 51474
Mutations
1,534
CL 158 · Tissue 1,338
Samples
282
CL 48 · Tissue 225
Peptides
266
unique mutant peptides
Transcripts
7
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
Mutations1,5341581,338
Samples28248225
Peptides26640225

Function

LIMA1 · LIM domain and actin binding 1

This gene encodes a cytoskeleton-associated protein that inhibits actin filament depolymerization and cross-links filaments in bundles. It is downregulated in some cancer cell lines. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, and expression of some of the variants maybe independently regulated. [provided by RefSeq, Aug 2011].

Isoforms & Proteins

7 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
ENST00000341247 Q9UHB6 305 237
ENST00000394943 Q9UHB6-4 275 221
ENST00000552823 Q9UHB6-2 212 167
ENST00000552783 Q9UHB6-5 211 166
ENST00000552909 F8VQE1* 211 166
ENST00000547825 Q9UHB6-3 160 125
ENST00000552491 F8VS07* 160 125

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q13.12
Entrez ID
Aliases
EPLINLDLCQ8SREBP3

Recurrent Mutations

All 237 amino-acid changes on canonical ENST00000341247 · 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 LIMA1 · 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 LIMA1 – 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
Oral Cavity Carcinoma
3/54 6%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Unknown
0/10 0%
1/29 3%
Endometrial Carcinoma
2/42 5%
14/612 2%
Germ Cell Tumour
2/25 8%
2/169 1%
Melanoma
4/210 2%
24/1899 1%
Bladder Carcinoma
1/58 2%
12/956 1%
Plasma Cell Myeloma
3/44 7%
1/305 0%
Squamous Cell Lung Carcinoma
5/57 9%
5/810 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Colorectal Carcinoma
4/143 3%
32/3239 1%
Gastric Carcinoma
0/74 0%
17/1809 1%
Other Solid Cancers
1/94 1%
12/1515 1%
Esophageal Carcinoma
1/23 4%
5/769 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Non-Small Cell Lung Carcinoma
1/304 0%
11/1390 1%
Biliary Tract Carcinoma
1/54 2%
6/950 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Other Sarcomas
1/69 1%
4/699 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Ovarian Carcinoma
2/109 2%
4/998 0%
Head and Neck Carcinoma
2/85 2%
7/1574 0%
Breast Carcinoma
0/144 0%
18/3264 1%
Glioma
0/52 0%
10/2127 0%
Mesothelioma
1/62 2%
0/165 0%
Thyroid Gland Carcinoma
2/45 4%
5/1592 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
8/2550 0%
Kidney Carcinoma
1/85 1%
4/1862 0%
Prostate Carcinoma
2/13 15%
3/2105 0%

Mutation Distribution

Where LIMA1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LIMA1 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 1,534 mutations in LIMA1

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