ITPR1

Inositol 1,4,5-trisphosphate receptor type 1 Q14643 ITPR1_HUMAN
Protein Coding Chr 3 3p26.1 Swiss-Prot reviewed Entrez 3708
Mutations
5,729
CL 779 · Tissue 4,889
Samples
1,200
CL 239 · Tissue 943
Peptides
1,153
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
Mutations5,7297794,889
Samples1,200239943
Peptides1,153205968

Function

ITPR1 · Inositol 1,4,5-trisphosphate receptor type 1

This gene encodes an intracellular receptor for inositol 1,4,5-trisphosphate. Upon stimulation by inositol 1,4,5-trisphosphate, this receptor mediates calcium release from the endoplasmic reticulum. Mutations in this gene cause spinocerebellar ataxia type 15, a disease associated with an heterogeneous group of cerebellar disorders. Multiple transcript variants have been identified for this gene. [provided by RefSeq, Nov 2009].

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
ENST00000443694 Q14643-2 1,267 955
ENST00000357086 Q14643-3 1,250 941
ENST00000456211 Q14643-4 1,244 936
ENST00000649015 Q14643 1,032 737
ENST00000354582 A0A3F2YNW8* 482 358
ENST00000544951 B7ZMI3* 305 244
ENST00000302640 A0A8C8KBY2* 149 115

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p26.1
Entrez ID
Aliases
ACVCLA4INSP3R1IP3RIP3R1PPP1R94

Recurrent Mutations

All 955 amino-acid changes on canonical ENST00000443694 · 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 ITPR1 · 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 ITPR1 – 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
8/40 20%
0/0 0%
Endometrial Carcinoma
13/42 31%
64/612 10%
Melanoma
24/210 11%
160/1899 8%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Hodgkins Lymphoma
7/16 44%
3/122 2%
Glioblastoma
7/98 7%
0/0 0%
Colorectal Carcinoma
29/143 20%
133/3239 4%
Other Solid Cancers
7/94 7%
69/1515 5%
Gastric Carcinoma
5/74 7%
77/1809 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Non-Small Cell Lung Carcinoma
22/304 7%
40/1390 3%
Bladder Carcinoma
8/58 14%
29/956 3%
Cervical Carcinoma
5/35 14%
10/422 2%
Neuroendocrine Tumour
11/154 7%
9/577 2%
Unknown
0/10 0%
1/29 3%
Squamous Cell Lung Carcinoma
2/57 4%
20/810 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Head and Neck Carcinoma
3/85 4%
31/1574 2%
Ovarian Carcinoma
13/109 12%
9/998 1%
Other Sarcomas
5/69 7%
10/699 1%
Non-Cancerous
3/104 3%
15/830 2%
Hepatocellular Carcinoma
0/46 0%
43/2210 2%
Biliary Tract Carcinoma
1/54 2%
18/950 2%
Mesothelioma
3/62 5%
1/165 1%
Small Cell Lung Carcinoma
1/9 11%
11/752 1%
Ewings Sarcoma
5/63 8%
0/262 0%
Rhabdomyosarcoma
3/33 9%
0/171 0%
Plasma Cell Myeloma
2/44 5%
3/305 1%
Osteosarcoma
2/45 4%
1/166 1%
Glioma
4/52 8%
26/2127 1%

Mutation Distribution

Where ITPR1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ITPR1 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 5,729 mutations in ITPR1

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