CARHSP1

Calcium regulated heat stable protein 1 Q9Y2V2 CHSP1_HUMAN
Protein Coding Chr 16 16p13.2 Swiss-Prot reviewed Entrez 23589
Mutations
759
CL 56 · Tissue 703
Samples
84
CL 13 · Tissue 71
Peptides
62
unique mutant peptides
Transcripts
10
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
Mutations75956703
Samples841371
Peptides62954

Function

CARHSP1 · Calcium regulated heat stable protein 1

Enables mRNA 3'-UTR binding activity. Predicted to be involved in regulation of mRNA stability. Predicted to be located in P granule and cytosol. Predicted to be active in cytoplasm. Predicted to colocalize with cytoplasmic exosome (RNase complex). [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

10 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
ENST00000311052 Q9Y2V2 86 57
ENST00000396593 Q9Y2V2 78 54
ENST00000561530 Q9Y2V2 78 54
ENST00000567554 Q9Y2V2 78 54
ENST00000610831 Q9Y2V2 78 54
ENST00000611932 Q9Y2V2 78 54
ENST00000614449 Q9Y2V2 78 54
ENST00000618335 Q9Y2V2 78 54
ENST00000619881 Q9Y2V2 78 54
ENST00000562843 I3L3X8* 49 35

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p13.2
Entrez ID
Aliases
CRHSP-24CRHSP24CSDC1

Recurrent Mutations

All 57 amino-acid changes on canonical ENST00000311052 · 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 CARHSP1 · 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 CARHSP1 – 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%
4/612 1%
Gastric Carcinoma
0/74 0%
9/1809 0%
Melanoma
0/210 0%
10/1899 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Colorectal Carcinoma
0/143 0%
13/3239 0%
Non-Cancerous
1/104 1%
2/830 0%
Other Solid Cancers
2/94 2%
3/1515 0%
Bladder Carcinoma
2/58 3%
1/956 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
4/2550 0%
Medulloblastoma
0/0 0%
1/450 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Non-Small Cell Lung Carcinoma
3/304 1%
0/1390 0%
Glioma
0/52 0%
4/2127 0%
Neuroblastoma
0/87 0%
2/1331 0%
Other Sarcomas
0/69 0%
1/699 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Ovarian Carcinoma
1/109 1%
0/998 0%
Thyroid Gland Carcinoma
0/45 0%
1/1592 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Prostate Carcinoma
0/13 0%
1/2105 0%

Mutation Distribution

Where CARHSP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CARHSP1 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 759 mutations in CARHSP1

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