ULK1

Unc-51 like autophagy activating kinase 1 O75385 ULK1_HUMAN
Protein Coding Chr 12 12q24.33 Swiss-Prot reviewed Entrez 8408
Mutations
647
CL 164 · Tissue 474
Samples
577
CL 139 · Tissue 431
Peptides
442
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
Mutations647164474
Samples577139431
Peptides44284372

Function

ULK1 · Unc-51 like autophagy activating kinase 1

Enables identical protein binding activity; protein serine/threonine kinase activity; and small GTPase binding activity. Involved in several processes, including autophagosome assembly; positive regulation by symbiont of host autophagy; and protein phosphorylation. Located in autophagosome; cytosol; and phagophore assembly site membrane. Is extrinsic component of autophagosome membrane; extrinsic component of omegasome membrane; and extrinsic component of phagophore assembly site membrane. Part of Atg1/ULK1 kinase complex. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000321867 O75385 647 442

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12q24.33
Entrez ID
Aliases
ATG1ATG1AUNC51Unc51.1hATG1

Recurrent Mutations

All 442 amino-acid changes on canonical ENST00000321867 · 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 ULK1 · 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 ULK1 – 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
10/40 25%
0/0 0%
Chronic Myelogenous Leukemia
5/25 20%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
3/26 12%
0/0 0%
Thymic Epithelial Tumor
0/0 0%
2/39 5%
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Endometrial Carcinoma
5/42 12%
20/612 3%
Melanoma
8/210 4%
61/1899 3%
Gastric Carcinoma
3/74 4%
47/1809 3%
Unknown
1/10 10%
0/29 0%
Non-Small Cell Lung Carcinoma
17/304 6%
23/1390 2%
Squamous Cell Lung Carcinoma
1/57 2%
19/810 2%
Colorectal Carcinoma
16/143 11%
57/3239 2%
Glioblastoma
2/98 2%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Thyroid Gland Carcinoma
2/45 4%
27/1592 2%
Bladder Carcinoma
2/58 3%
14/956 1%
Cervical Carcinoma
1/35 3%
6/422 1%
Other Sarcomas
6/69 9%
5/699 1%
Other Solid Cancers
3/94 3%
20/1515 1%
Germ Cell Tumour
1/25 4%
1/169 1%
Glioma
1/52 2%
20/2127 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Hepatocellular Carcinoma
0/46 0%
19/2210 1%
Ovarian Carcinoma
4/109 4%
5/998 0%
B-Cell Non-Hodgkins Lymphoma
8/88 9%
12/2534 0%
Esophageal Carcinoma
0/23 0%
6/769 1%
Non-Cancerous
4/104 4%
3/830 0%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Head and Neck Carcinoma
1/85 1%
11/1574 1%

Mutation Distribution

Where ULK1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ULK1 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 647 mutations in ULK1

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