DEPP1

DEPP autophagy regulator 1 Q9NTK1 DEPP1_HUMAN
Protein Coding Chr 10 10q11.21 Swiss-Prot reviewed Entrez 11067
Mutations
108
CL 32 · Tissue 74
Samples
107
CL 32 · Tissue 73
Peptides
77
unique mutant peptides
Transcripts
1
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
Mutations1083274
Samples1073273
Peptides771960

Function

DEPP1 · DEPP autophagy regulator 1

The expression of this gene is induced by fasting as well as by progesterone. The protein encoded by this gene contains a t-synaptosome-associated protein receptor (SNARE) coiled-coil homology domain and a peroxisomal targeting signal. Production of the encoded protein leads to phosphorylation and activation of the transcription factor ELK1. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000298295 Q9NTK1 108 77

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q11.21
Entrez ID
Aliases
C10orf10DEPPFIGFseg

Recurrent Mutations

All 77 amino-acid changes on canonical ENST00000298295 · 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 DEPP1 · 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 DEPP1 – 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%
Chondrosarcoma
1/14 7%
0/75 0%
Endometrial Carcinoma
1/42 2%
5/612 1%
Melanoma
2/210 1%
14/1899 1%
Squamous Cell Lung Carcinoma
2/57 4%
3/810 0%
Gastric Carcinoma
2/74 3%
7/1809 0%
Ovarian Carcinoma
5/109 5%
0/998 0%
Colorectal Carcinoma
8/143 6%
6/3239 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Glioma
0/52 0%
7/2127 0%
Non-Cancerous
0/104 0%
3/830 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Non-Small Cell Lung Carcinoma
2/304 1%
2/1390 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Hepatocellular Carcinoma
1/46 2%
3/2210 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Bladder Carcinoma
0/58 0%
1/956 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
1/2534 0%
Other Blood Cancers
0/61 0%
2/2725 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
Breast Carcinoma
1/144 1%
0/3264 0%

Mutation Distribution

Where DEPP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DEPP1 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.

Mutations

All 108 mutations in DEPP1

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