LYRM1

LYR motif containing 1 O43325 LYRM1_HUMAN
Protein Coding Chr 16 16p12.3 Swiss-Prot reviewed Entrez 57149
Mutations
302
CL 41 · Tissue 242
Samples
50
CL 9 · Tissue 37
Peptides
37
unique mutant peptides
Transcripts
8
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
Mutations30241242
Samples50937
Peptides37730

Function

LYRM1 · LYR motif containing 1

The protein encoded by this gene belongs to the mitochondrial leucine/tyrosine/arginine motif family of proteins. Proteins of this family are short polypeptides that contain a leucine/tyrosine/arginine motif near the N-terminus. This gene is widely expressed with high levels in omental adipose tissue of obese individuals. In adipose tissue, the protein is localized to the nucleus where it promotes preadipocyte proliferation and lowers the rate of apoptosis to regulate adipose tissue homeostasis. Overexpression of this gene in adipocytes causes abnormal mitochondrial morphology and mitochondrial dysfunction. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014].

Isoforms & Proteins

8 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
ENST00000567954 O43325 50 33
ENST00000219168 O43325 46 31
ENST00000396052 O43325 46 31
ENST00000439021 O43325 46 31
ENST00000568663 O43325 46 31
ENST00000569023 O43325 46 31
ENST00000412082 H3BNA8* 11 8
ENST00000562740 H3BNA8* 11 8

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p12.3
Entrez ID
Aliases
A211C6.1

Recurrent Mutations

All 33 amino-acid changes on canonical ENST00000567954 · 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 LYRM1 · 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 LYRM1 – 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
2/40 5%
0/0 0%
Endometrial Carcinoma
0/42 0%
5/612 1%
Ovarian Carcinoma
1/109 1%
3/998 0%
Melanoma
0/210 0%
6/1899 0%
Other Sarcomas
0/69 0%
2/699 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Colorectal Carcinoma
0/143 0%
7/3239 0%
Other Solid Cancers
1/94 1%
2/1515 0%
Non-Small Cell Lung Carcinoma
2/304 1%
1/1390 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
3/2550 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Neuroblastoma
1/87 1%
0/1331 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where LYRM1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LYRM1 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 302 mutations in LYRM1

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