CDIP1

Cell death inducing p53 target 1 Q9H305 CDIP1_HUMAN
Protein Coding Chr 16 16p13.3 Swiss-Prot reviewed Entrez 29965
Mutations
276
CL 29 · Tissue 241
Samples
66
CL 13 · Tissue 51
Peptides
83
unique mutant peptides
Transcripts
6
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
Mutations27629241
Samples661351
Peptides831565

Function

CDIP1 · Cell death inducing p53 target 1

Predicted to enable metal ion binding activity. Acts upstream of or within intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator and tumor necrosis factor-mediated signaling pathway. Located in cytoplasmic side of late endosome membrane; cytoplasmic side of lysosomal membrane; and nucleus. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

6 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
ENST00000567695 Q9H305 66 54
ENST00000399599 Q9H305 56 47
ENST00000563332 Q9H305 56 47
ENST00000563507 Q9H305-2 48 40
ENST00000562334 Q9H305-3 30 25
ENST00000564828 H3BRY7* 20 17

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p13.3
Entrez ID
Aliases
C16orf5CDIPI1LITAFL

Recurrent Mutations

All 54 amino-acid changes on canonical ENST00000567695 · 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 CDIP1 · 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 CDIP1 – 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
Glioblastoma
1/98 1%
0/0 0%
Mesothelioma
1/62 2%
1/165 1%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Osteosarcoma
1/45 2%
0/166 0%
Colorectal Carcinoma
4/143 3%
11/3239 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Melanoma
1/210 0%
5/1899 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Glioma
0/52 0%
4/2127 0%
Endometrial Carcinoma
0/42 0%
1/612 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
Gastric Carcinoma
0/74 0%
2/1809 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Prostate Carcinoma
2/13 15%
0/2105 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where CDIP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CDIP1 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 276 mutations in CDIP1

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