LRRC27

Leucine rich repeat containing 27 Q9C0I9 LRC27_HUMAN
Protein Coding Chr 10 10q26.3 Swiss-Prot reviewed Entrez 80313
Mutations
1,002
CL 94 · Tissue 900
Samples
268
CL 38 · Tissue 228
Peptides
223
unique mutant peptides
Transcripts
5
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
Mutations1,00294900
Samples26838228
Peptides22332198

Isoforms & Proteins

5 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
ENST00000368614 Q9C0I9 242 179
ENST00000368613 Q9C0I9 226 171
ENST00000368612 Q9C0I9-2 196 149
ENST00000344079 Q9C0I9-3 172 125
ENST00000625755 Q9C0I9-4 166 124

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q26.3
Entrez ID

Recurrent Mutations

All 179 amino-acid changes on canonical ENST00000368614 · 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 LRRC27 · 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 LRRC27 – 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
2/54 4%
0/0 0%
Endometrial Carcinoma
0/42 0%
24/612 4%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Melanoma
2/210 1%
31/1899 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Cervical Carcinoma
0/35 0%
6/422 1%
Colorectal Carcinoma
5/143 4%
39/3239 1%
Squamous Cell Lung Carcinoma
3/57 5%
6/810 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Gastric Carcinoma
1/74 1%
17/1809 1%
Other Sarcomas
0/69 0%
5/699 1%
Hepatocellular Carcinoma
2/46 4%
11/2210 0%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Ovarian Carcinoma
1/109 1%
5/998 0%
Non-Cancerous
0/104 0%
5/830 1%
Non-Small Cell Lung Carcinoma
6/304 2%
3/1390 0%
Bladder Carcinoma
0/58 0%
5/956 1%
Head and Neck Carcinoma
1/85 1%
7/1574 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
9/2534 0%
Biliary Tract Carcinoma
1/54 2%
3/950 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Thyroid Gland Carcinoma
2/45 4%
4/1592 0%
Breast Carcinoma
2/144 1%
10/3264 0%
Kidney Carcinoma
1/85 1%
5/1862 0%
Pancreatic Carcinoma
0/89 0%
5/1611 0%
Glioma
0/52 0%
6/2127 0%
Other Blood Cancers
3/61 5%
3/2725 0%
Medulloblastoma
0/0 0%
1/450 0%
Other Solid Cancers
0/94 0%
3/1515 0%

Mutation Distribution

Where LRRC27 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LRRC27 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 1,002 mutations in LRRC27

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