LIMCH1 LIM and calponin homology domains 1 Q9UPQ0 LIMC1_HUMAN
Protein Coding Chr 4 4p13 Swiss-Prot reviewed Entrez 22998
Mutations
7,101
CL 645 · Tissue 6,164
Samples
729
CL 153 · Tissue 551
Peptides
652
unique mutant peptides
Transcripts
14
isoforms mutated

Stats by Source

Global, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Global = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Global can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

GlobalCell lineTissue
Mutations7,1016456,164
Samples729153551
Peptides652122543

Function

LIMCH1 · LIM and calponin homology domains 1

Enables myosin II head/neck binding activity. Involved in several processes, including cytoplasmic actin-based contraction involved in cell motility; positive regulation of stress fiber assembly; and regulation of focal adhesion assembly. Located in stress fiber. Colocalizes with myosin II complex. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

14 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
ENST00000503057 G5EA03* 756 508
ENST00000313860 Q9UPQ0 620 443
ENST00000512946 Q9UPQ0-2 597 426
ENST00000512820 Q9UPQ0-4 596 425
ENST00000508501 Q9UPQ0-10 595 425
ENST00000509277 E9PDJ9* 542 386
ENST00000512632 D6RD46* 540 389
ENST00000513024 Q9UPQ0-5 534 379
ENST00000396595 Q9UPQ0-6 533 379
ENST00000511496 Q9UPQ0-8 533 379
ENST00000381753 Q9UPQ0-9 524 373
ENST00000514096 E7EPK0* 523 372
ENST00000509454 F6V7S8* 104 75
ENST00000509638 D6RJ93* 104 75

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4p13
Entrez ID
Aliases
LIMCH1ALMO7B

Recurrent Mutations

Top recurrent amino-acid changes along the protein · needle height = number of mutations

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 Distribution

Where LIMCH1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LIMCH1 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 7,101 mutations in LIMCH1

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 CDSTypeSourcePeptide